Laccase mutants

ABSTRACT

The present invention relates to a method of designing laccase mutants with increased oxidation potential and/or changed pH optimum and/or altered mediator pathway and/or altered O 2  /OH -  -pathway, which method is based on the three-dimensional structure of laccases.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority of Danish application 0222/97 filedFeb. 28, 1997, the contents of which are fully incorporated herein byreference.

FIELD OF THE INVENTION

The present invention relates to a method of designing laccase mutantswith increased oxidation potential and/or changed pH optimum and/oraltered mediator pathway and/or altered O₂ /OH⁻ -pathway, which methodis based on the hitherto unknown three-dimensional structure oflaccases.

BACKGROUND OF THE INVENTION

Laccase is a polyphenol oxidase (EC 1.10.3.2) which catalyses theoxidation of a variety of inorganic and aromatic compounds, particularlyphenols, with the concomitant reduction of molecular oxygen to water.

Laccase belongs to a family of blue copper-containing oxidases whichincludes ascorbate oxidase and the mammalian plasma proteinceruloplasmin. All these enzymes are multi-copper-containing proteins.

Because laccases are able to catalyze the oxidation of a variety ofinorganic and aromatic compounds, laccases have been suggested in manypotential industrial applications such as lignin modification, paperstrengthening, dye transfer inhibition in detergents, phenolpolymerization, hair colouring, and waste water treatment.

No three-dimensional structural information has been available for alaccase before.

We have now elucidated the three-dimensional structure of a Coprinuscinereus laccase. By having this three-dimensional structure we are ableto create laccase variants with altered properties: increased oxidationpotential and/or changed pH optimum and/or altered mediator pathwayand/or altered O₂ /OH⁻ -pathway.

BRIEF DISCLOSURE OF THE INVENTION

The three-dimensional structure of a laccase has now been elucidated. Onthe basis of an analysis of said structure it is possible to identifystructural parts or specific amino acid residues which from structuralor functional considerations appear to be important for increasedoxidation potential and/or changed pH optimum and/or altered mediatorpathway and/or altered O₂ /OH⁻ -pathway of a laccase.

Furthermore, when comparing the three-dimensional structure of theCoprinus laccase structure with known amino acid sequences of variouslaccases, it has been found that some similarities exist between thesequences. The present invention is based on these findings.

Accordingly, in a first aspect the invention relates to a method ofconstructing a variant of a parent Coprinus laccase, which variant haslaccase activity and increased oxidation potential and/or changed pHoptimum and/or altered mediator pathway and/or altered O₂ /OH⁻ -pathwayas compared to said parent laccase, which method comprises

i) analysing the three-dimensional structure of the parent Coprinuslaccase to identify at least one amino acid residue or at least onestructural part of the Coprinus laccase structure, which amino acidresidue or structural part is believed to be of relevance for alteringthe oxidation potential and/or altering the pH optimum and/or alteringthe mediator pathway and/or altering the O₂ /OH⁻ -pathway of the parentCoprinus laccase (as evaluated on the basis of structural or functionalconsiderations),

ii) constructing a Coprinus laccase variant, which as compared to theparent Coprinus laccase, has been modified in the amino acid residue orstructural part identified in i) so as to alter the oxidation potentialand/or alter the pH optimum and/or alter the mediator pathway and/oralter the O₂ /OH⁻ -pathway, and, optionally,

iii) testing the resulting Coprinus laccase variant with respect tooxidation potential and/or pH optimum and/or mediator pathway and/or O₂/OH⁻ -pathway.

In a second aspect the present invention relates to a method ofconstructing a variant of a parent Coprinus-like laccase, which varianthas laccase activity and increased oxidation potential and/or changed pHoptimum and/or altered mediator pathway and/or altered O₂ /OH⁻ -pathwayas compared to said parent laccase, which method comprises

i) comparing the three-dimensional amino acid structure of the Coprinuslaccase with an amino acid sequence of a Coprinus-like laccase,

ii) identifying a part of the Coprinus-like laccase amino acid sequencewhich is different from the Coprinus laccase amino acid sequence andwhich from structural or functional considerations is contemplated to beresponsible for differences in the stability of the Coprinus andCoprinus-like laccase,

iii) modifying the part of the Coprinus-like laccase identified in ii)whereby a Coprinus-like laccase variant is obtained, which has anincreased oxidation potential and/or changed pH optimum and/or alteredmediator pathway and/or altered O₂ /OH⁻ -pathway as compared to theparent Coprinus-like laccase, and optionally,

iv) testing the resulting Coprinus-like laccase variant with respect tooxidation potential and/or pH optimum and/or mediator pathway and/or O₂/OH⁻ -pathway.

In still further aspects the invention relates to variants of a Coprinuslaccase and of Coprinus-like laccases, DNA encoding such variants andmethods of preparing the variants. Finally, the invention relates to theuse of the variants for various industrial purposes.

DETAILED DISCLOSURE OF THE INVENTION The Coprinus-like Laccases

A number of laccases produced by different fungi are homologous on theamino acid level. For instance, when using the 35 homology percentobtained from UWGCG program using the GAP program with the defaultparameters (penalties: gap weight=3.0, length weight=0.1; WISCONSINPACKAGE Version 8.1-UNIX, August 1995, Genetics Computer Group, 575Science Drive, Madison, Wis., USA 53711) the following homology wasfound:

Coprinus cinereus laccase comprising the amino acid sequence shown inSEQ ID No. 1: 100%;

Polyporus pinsitus (I) laccase comprising the amino acid sequence shownin SEQ ID No. 2: 74.4%;

Polyporus pinsitus (II) laccase comprising the amino acid sequence shownin SEQ ID No. 3: 73.8%;

Phlebia radiata laccase comprising the amino acid sequence shown in SEQID No. 4: 69.9%;

Rhizoctonia solani (I) laccase comprising the amino acid sequence shownin SEQ ID No. 5: 64.8%;

Rhizoctonia solani (II) laccase comprising the amino acid sequence shownin SEQ ID No. 6: 63.0%;

Rhizoctonia solani (III) laccase comprising the amino acid sequenceshown in SEQ ID No. 7: 61.0%;

Rhizoctonia solani (IV) laccase comprising the amino acid sequence shownin SEQ ID No. 8: 59.7%;

Scytalidium thermophilum laccase comprising the amino acid sequenceshown in SEQ ID No. 9: 57.4%;

Myceliophthora thermophila laccase comprising the amino acid sequenceshown in SEQ ID No. 10: 56.5%.

Because of the homology found between the above mentioned laccases, theyare considered to belong to the same class of laccases, namely the classof "Coprinus-like laccases".

Accordingly, in the present context, the term "Coprinus-like laccase" isintended to indicate a laccase which, on the amino acid level, displaysa homology of at least 50% and less than 100% to the Coprinus cinereuslaccase SEQ ID NO 1, or at least 55% and less than 100% to the Coprinuscinereus laccase SEQ ID NO 1, or at least 60% and less than 100% to theCoprinus cinereus laccase SEQ ID NO 1, or at least 65% and less than100% to the Coprinus cinereus laccase SEQ ID NO 1, or at least 70% andless than 100% to the Coprinus cinereus laccase SEQ ID NO 1, or at least75% and less than 100% to the Coprinus cinereus laccase SEQ ID NO 1, orat least 80% and less than 100% to the Coprinus cinereus laccase SEQ IDNO 1, or at least 85% and less than 100% to the Coprinus cinereuslaccase SEQ ID NO 1, or at least 90% and less than 100% to the Coprinuscinereus laccase SEQ ID NO 1, or at least 95% and less than 100% to theCoprinus cinereus laccase SEQ ID NO 1.

In the present context, "derived from" is intended not only to indicatea laccase produced or producible by a strain of the organism inquestion, but also a laccase encoded by a DNA sequence isolated fromsuch strain and produced in a host organism containing said DNAsequence. Finally, the term is intended to indicate a laccase which isencoded by a DNA sequence of synthetic and/or cDNA origin and which hasthe identifying characteristics of the laccase in question.

The Three-dimensional Coprinus Laccase Structure

The Coprinus laccase which was used to elucidate the three-dimensionalstructure forming the basis for the present invention consists of the539 amino acids derived from Coprinus cinereus laccase IFO 8371 asdisclosed in sequence ID No. 1.

The obtained three-dimensional structure is believed to berepresentative for the structure of any Coprinus-like laccase.

The structure of the laccase was solved in accordance with the principlefor X-ray crystallographic methods given in "X-Ray StructureDetermination", Stout, G. K. and Jensen, L. H., John Wiley & Sons, inc.N.Y., 1989. The structural coordinates for the solved crystal structureof the laccase at 2.2 Å resolution using the isomorphous replacementmethod are given in a standard PDB format (Brookhaven Protein Data Base)in Appendix 1. It is to be understood that Appendix 1 forms part of thepresent application.

In Appendix 1 the amino acid residues of the enzyme are identified bythree-letter amino acid code (capitalized letters).

The laccase structure is made up of three plastocyanin-like domains.These three domains all have a similar beta-barrel fold.

3 copper atoms were observed in the three-dimensional structure:

The so-called type 1 copper ion is coordinated by two histidines and onecysteine.

The so-called type 2 copper of the trinuclear centre is missing in thestructure disclosed in the present application.

The so-called type 3 copper consists of two type 3 copper atoms (pair ofcopper atoms) bound to a total of 6 histidine ligands.

When comparing the amino acid sequence of the crystallizedthree-dimensional structure with Coprinus cinereus amino acid sequenceID No. 1 the following four differences are observed:

18 amino acids are missing from the N-terminal of the crystallizedprotein;

17 amino acids are missing from the C-terminal of the crystallizedprotein;

Q19 in sequence ID No. 1 is an A1 in the crystallized protein; and

Q243 in sequence ID No. 1 is an E225 in the crystallized protein.

Generality of Structure

Because of the homology between the Coprinus laccase and the variousCoprinus-like laccases, the solved structure defined by the coordinatesof Appendix 1 is believed to be representative for the structure of allCoprinus-like laccases. A model structure of Coprinus-like laccases maybe built on the basis of the coordinates given in Appendix 1 adapted tothe laccase in question by use of an alignment between the respectiveamino acid sequences.

The above identified structurally characteristic parts of the Coprinuslaccase structure may be identified in other Coprinus-like laccases onthe basis of a model (or solved) structure of the relevant Coprinus-likelaccase or simply on the basis of an alignment between the amino acidsequence of the Coprinus-like laccase in question with that of theCoprinus laccase used herein for identifying the amino acid residues ofthe respective structural elements.

Furthermore, in connection with Coprinus laccase variants of theinvention, which are defined by modification of specific amino acidresidues of the parent Coprinus laccase, it will be understood thatvariants of Coprinus-like laccases modified in an equivalent position(as determined from the best possible amino acid sequence alignmentbetween the respective sequences) are intended to be covered as well.

Methods of the Invention for Design of Novel Laccase Variants

The analysis or comparison performed in step i) of the methods of theinvention may be performed by use of any suitable computer programcapable of analyzing and/or comparing amino acid sequences.

The structural part which is identified in step i) of the methods of theinvention may be composed of one amino acid residue. However, normallythe structural part comprises more than one amino acid residue,typically constituting one of the above mentioned parts of the Coprinusstructure such as one of the copper centers.

Modifications

The modification of an amino acid residue or structural part istypically accomplished by suitable modifications of a DNA sequenceencoding the parent enzyme in question. The term "modified" as used inthe methods according to the invention is intended to have the followingmeaning: When used in relation to an amino acid residue the term isintended to mean replacement of the amino acid residue in question withanother amino acid residue. When used in relation to a structural part,the term is intended to mean: replacement of one or more amino acidresidues of said structural part with other amino acid residues, oraddition of one or more amino acid residues to said part, or deletion ofone or more amino acid residues of said structural part.

The construction of the variant of interest is accomplished bycultivating a microorganism comprising a DNA sequence encoding thevariant under conditions which are conducive for producing the variant,and optionally subsequently recovering the variant from the resultingculture broth. This is described in detail further below.

Variants with Altered Oxidation Potential

The redox potentials of various wild type laccases have been found to bethe following (measured at pH 5.3):

    ______________________________________                                                              E°, V vs NHE                                     ______________________________________                                        Coprinus cinereus (SEQ ID No. 1):                                                                     0.55                                                    Polyporus pinsitus (SEQ ID No. 2): 0.79                                       Myceliophthora thermophila (SEQ ID No. 10): 0.48                              Rhizoctonia solani (SEQ ID No. 7): 0.75                                       Scytalidium thermophilum (SEQ ID No. 9): 0.53                               ______________________________________                                    

It is contemplated that it is possible to increase the oxidationpotential of a parent Coprinus laccase or a parent Coprinus-likelaccase, wherein said variant is the result of a mutation, i.e. one ormore amino acid residues have been deleted from, replaced or added tothe parent laccase. Preferred positions for mutations are the following:

Coprinus cinereus laccase (SEQ ID No. 1):

G411A,V,P,L,I,F,Y,W;

G412A,V,P,L,I,F,Y,W;

V409P,L,I,F,Y,W;

T257A,V,P,L,I,F,Y,W;

F358Y,W,I;

T359A,V,P,L,I,F,Y,W;

L480I,F,Y,W;

L351I,F,Y,W;

E473A,V,P,L,I,F,Y,W;

D98A,V,P,L,I,F,Y,W;

G131A,V,P,L,I,F,Y,W;

D443A,V,P,L,I,F,Y,W;

R260 A,V,P,L,I,F,Y,W; in particular

G411A,V;

G412A,V,L,I;

V409L,I;

T257V;

F358W;

T359V,F;

L480I,F;

L351I,F;

E473L,I,F;

D98L,I,F;

G131V,L,I;

D443I,F;

R260I;

D443I+R260I;

D443F+R260I.

Polyporus pinsitus (SEQ ID No. 2):

A390V,P,L,I,F,Y,W;

G392A,V,P,L,I,F,Y,W;

E460D; in particular

A390V,L,I;

G392A,V.

Myceliophthora thermophila laccase (SEQ ID No. 10):

G511A,V,P,L,I,F,Y,W;

T428A,V,P,L,I,F,Y,W;

S510A,V,P,L,I,F,Y,W;

D106A,V,P,L,I,F,Y,W;

N109A,V,P,L,I,F,Y,W,Q;

L500I,F,Y,W;

A108V,P,L,I,F,Y,W;

G514A,V,P,L,I,F,Y,W; in particular

G511A,V,L,I,F;

T428V;

S510V;

D106L;

N109I,F,Q;

L500F;

A108V,I;

G514A,V,L,I,F.

Preferred variants include any combination of the above mentionedmutations.

Variants with Altered pH Optimum

The desired pH optimum of a laccase depends on which application is ofinterest, e.g., if the laccase is to be used for denim bleaching thepreferred pH optimum will be around pH 5-8, whereas if the laccase is tobe used for washing purposes the preferred pH optimum will be around pH8-10.

It is contemplated that it is possible to alter the pH optimum of aparent Coprinus laccase or a parent Coprinus-like laccase by creating amutation in an amino acid within 10 Å from the active His in the Cu1site.

Preferred positions for mutations are the following:

Coprinus cinereus laccase (SEQ ID No. 1):

180-181;

222-224;

257;

281-284;

352-353;

357-358;

409-416;

470-490.

Polyporus pinsitus (SEQ ID No. 2):

E460L,I,F,M,S;

F463L,M.

Myceliophthora thermophila (SEQ ID No. 10):

192-193;

234-236;

269;

293-294;

364-365;

372-373;

426-433;

503-513.

Preferred substitutions are the following: E, D, L, I, F, Y, W.

Variants with Altered Mediator Efficiency

Laccases are often used in combination with so called mediators orenhancers, e.g., in combination with phenothiazine or phenothiazinerelated compounds (see WO 95/01426) or in combination withacetosyringone or acetosyringone related compounds (see WO 96/10079).

It is contemplated that it is possible to alter the mediator efficiency(in order to make the mediator more efficient), of a parent Coprinuslaccase or a parent Coprinus-like laccase by creating a mutation in anamino acid in one or more of the following positions:

Coprinus cinereus laccase (SEQ ID No. 1):

179-182;

223;

281-282;

353-358;

410-412;

472;

474-475;

477-478.

Preferred substitutions are the following: W, F, M, Y, R, K, S, T, N, Q;in particular the following substitutions:

F358W;

N478Q.

Myceliophthora thermophila laccase (SEQ ID No. 10):

185-194;

235;

293-294;

365-373;

427-429;

505;

507-508;

510-511.

Preferred substitutions are in particular one or more of the followingmutations:

N189G,A,S,T;

S190G,A;

F371* (deletion);

F371G,A.

Polyporus pinsitus (SEQ ID No. 2):

G392A;

A461T,S;

N260Q,Y;

G165K,R.

Altered O₂ /OH⁻ -pathway

It is contemplated that it is possible to lower the possibility of OH⁻entering the trinuclear Cu site by producing one or more of thefollowing mutations:

Myceliophthora thermophila (SEQ ID No. 10):

A506E;

N109D;

H93E;

H95E;

M433E;

M480E.

Polyporus pinsitus (SEQ ID No. 2):

F81D,E;

L112D,E;

A80D,E.

Methods of Preparing Laccase Variants

Several methods for introducing mutations into genes are known in theart. After a brief discussion of the cloning of laccase-encoding DNAsequences, methods for generating mutations at specific sites within thelaccase-encoding sequence will be discussed.

Cloning a DNA Sequence Encoding a Laccase

The DNA sequence encoding a parent laccase may be isolated from any cellor microorganism producing the laccase in question, using variousmethods well known in the art. First, a genomic DNA and/or cDNA libraryshould be constructed using chromosomal DNA or messenger RNA from theorganism that produces the laccase to be studied. Then, if the aminoacid sequence of the laccase is known, homologous, labelledoligonucleotide probes may be synthesized and used to identifylaccase-encoding clones from a genomic library prepared from theorganism in question. Alternatively, a labelled oligonucleotide probecontaining sequences homologous to a known laccase gene could be used asa probe to identify laccase-encoding clones, using hybridization andwashing conditions of lower stringency.

A method for identifying laccase-encoding clones involves inserting cDNAinto an expression vector, such as a plasmid, transforminglaccase-negative fungi with the resulting cDNA library, and then platingthe transformed fungi onto agar containing a substrate for laccase,thereby allowing clones expressing the laccase to be identified.

Alternatively, the DNA sequence encoding the enzyme may be preparedsynthetically by established standard methods, e.g. the phosphoroamiditemethod. In the phosphoroamidite method, oligonucleotides aresynthesized, e.g. in an automatic DNA synthesizer, purified, annealed,ligated and cloned in appropriate vectors.

Finally, the DNA sequence may be of mixed genomic and synthetic origin,mixed synthetic and cDNA origin or mixed genomic and cDNA origin,prepared by ligating fragments of synthetic, genomic or cDNA origin (asappropriate, the fragments corresponding to various parts of the entireDNA sequence), in accordance with standard techniques. The DNA sequencemay also be prepared by polymerase chain reaction (PCR) using specificprimers.

Site-directed Mutagenesis

Once a laccase-encoding DNA sequence has been isolated, and desirablesites for mutation identified, mutations may be introduced usingsynthetic oligonucleotides. These oligonucleotides contain nucleotidesequences flanking the desired mutation sites; mutant nucleotides areinserted during oligonucleotide synthesis. In a specific method, asingle-stranded gap of DNA, bridging the laccase-encoding sequence, iscreated in a vector carrying the laccase gene. Then the syntheticnucleotide, bearing the desired mutation, is annealed to a homologousportion of the single-stranded DNA. The remaining gap is then filled inwith T7 DNA polymerase and the construct is ligated using T4 ligase. Aspecific example of this method is described in Morinaga et al. (1984).U.S. Pat. No. 4,760,025 discloses the introduction of oligonucleotidesencoding multiple mutations by performing minor alterations of thecassette. However, an even greater variety of mutations can beintroduced at any one time by the Morinaga method, because a multitudeof oligonucleotides, of various lengths, can be introduced.

Another method of introducing mutations into laccase-encoding DNAsequences is described in Nelson and Long (1989). It involves the 3-stepgeneration of a PCR fragment containing the desired mutation introducedby using a chemically synthesized DNA strand as one of the primers inthe PCR reactions. From the PCR-generated fragment, a DNA fragmentcarrying the mutation may be isolated by cleavage with restrictionendonucleases and reinserted into an expression plasmid.

Random Mutagenesis

The random mutagenesis of a DNA sequence encoding a parent laccase mayconveniently be performed by use of any method known in the art.

For instance, the random mutagenesis may be performed by use of asuitable physical or chemical mutagenizing agent, by use of a suitableoligonucleotide, or by subjecting the DNA sequence to PCR generatedmutagenesis. Furthermore, the random mutagenesis may be performed by useof any combination of these mutagenizing agents.

The mutagenizing agent may, e.g., be one which induces transitions,transversions, inversions, scrambling, deletions, and/or insertions.

Examples of a physical or chemical mutagenizing agent suitable for thepresent purpose include ultraviolet (UV) irradiation, hydroxylamine,N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), 0-methyl hydroxylamine,nitrous acid, ethyl methane sulphonate (EMS), sodium bisulphite, formicacid, and nucleotide analogues.

When such agents are used, the mutagenesis is typically performed byincubating the DNA sequence encoding the parent enzyme to be mutagenizedin the presence of the mutagenizing agent of choice under suitableconditions for the mutagenesis to take place, and selecting for mutatedDNA having the desired properties.

When the mutagenesis is performed by the use of an oligonucleotide, theoligonucleotide may be doped or spiked with the three non-parentnucleotides during the synthesis of the oligonucleotide at the positionswhich are to be changed. The doping or spiking may be done so thatcodons for unwanted amino acids are avoided. The doped or spikedoligonucleotide can be incorporated into the DNA encoding the laccaseenzyme by any published technique, using e.g. PCR, LCR or any DNApolymerase and ligase.

When PCR-generated mutagenesis is used, either a chemically treated ornon-treated gene encoding a parent laccase enzyme is subjected to PCRunder conditions that increase the misincorporation of nucleotides(Deshler 1992; Leung et al., Technique, Vol.1, 1989, pp. 11-15).

A mutator strain of E. coli (Fowler et al., Molec. Gen. Genet., 133,1974, pp. 179-191), S. cereviseae or any other microbial organism may beused for the random mutagenesis of the DNA encoding the laccase enzymeby e.g. transforming a plasmid containing the parent enzyme into themutator strain, growing the mutator strain with the plasmid andisolating the mutated plasmid from the mutator strain. The mutatedplasmid may subsequently be transformed into the expression organism.

The DNA sequence to be mutagenized may conveniently be present in agenomic or cDNA library prepared from an organism expressing the parentlaccase enzyme. Alternatively, the DNA sequence may be present on asuitable vector such as a plasmid or a bacteriophage, which as such maybe incubated with or otherwise exposed to the mutagenizing agent. TheDNA to be mutagenized may also be present in a host cell either by beingintegrated in the genome of said cell or by being present on a vectorharboured in the cell. Finally, the DNA to be mutagenized may be inisolated form. It will be understood that the DNA sequence to besubjected to random mutagenesis is preferably a cDNA or a genomic cDNAsequence.

In some cases it may be convenient to amplify the mutated DNA sequenceprior to the expression step or the screening step being performed. Suchamplification may be performed in accordance with methods known in theart, the presently preferred method being PCR-generated amplificationusing oligonucleotide primers prepared on the basis of the DNA or aminoacid sequence of the parent enzyme.

Subsequent to the incubation with or exposure to the mutagenizing agent,the mutated DNA is expressed by culturing a suitable host cell carryingthe DNA sequence under conditions allowing expression to take place. Thehost cell used for this purpose may be one which has been transformedwith the mutated DNA sequence, optionally present on a vector, or onewhich was carried the DNA sequence encoding the parent enzyme during themutagenesis treatment. Examples of suitable host cells are fungal hostssuch as Aspergillus niger or Aspergillus oryzae.

The mutated DNA sequence may further comprise a DNA sequence encodingfunctions permitting expression of the mutated DNA sequence.

Localized Random Mutagenesis

The random mutagenesis may advantageously be localized to a part of theparent laccase in question. This may, e.g., be advantageous when certainregions of the enzyme have been identified to be of particularimportance for a given property of the enzyme, and when modified areexpected to result in a variant having improved properties. Such regionsmay normally be identified when the tertiary structure of the parentenzyme has been elucidated and related to the function of the enzyme.

The localized random mutagenesis is conveniently performed by use ofPCR-generated mutagenesis techniques as described above or any othersuitable technique known in the art.

Alternatively, the DNA sequence encoding the part of the DNA sequence tobe modified may be isolated, e.g. by being inserted into a suitablevector, and said part may subsequently be subjected to mutagenesis byuse of any of the mutagenesis methods discussed above.

With respect to the screening step in the above-mentioned method of theinvention, this may conveniently be performed by use of aa filter assaybased on the following principle:

A microorganism capable of expressing the mutated laccase enzyme ofinterest is incubated on a suitable medium and under suitable conditionsfor the enzyme to be secreted, the medium being provided with a doublefilter comprising a first protein binding filter and on top of that asecond filter exhibiting a low protein binding capability. Themicroorganism is located on the second filter. Subsequent to theincubation, the first filter comprising enzymes secreted from themicroorganisms is separated from the second filter comprising themicroorganisms. The first filter is subjected to screening for thedesired enzymatic activity and the corresponding microbial coloniespresent on the second filter are identified.

The filter used for binding the enzymatic activity may be any proteinbinding filter e.g. nylon or nitrocellulose. The top filter carrying thecolonies of the expression organism may be any filter that has no or lowaffinity for binding proteins e.g. cellulose acetate or Durapore™. Thefilter may be pretreated with any of the conditions to be used forscreening or may be treated during the detection of enzymatic activity.

The enzymatic activity may be detected by a dye, fluorescence,precipitation, pH indicator, IR-absorbance or any other known techniquefor detection of enzymatic activity.

The detecting compound may be immobilized by any immobilizing agent,e.g., agarose, agar, gelatin, polyacrylamide, starch, filter paper,cloth; or any combination of immobilizing agents.

Laccase Activity

In the context of this invention, the laccase activity was measuredusing 10-(2-hydroxyethyl)-phenoxazine (HEPO) as substrate for thevarious laccases. HEPO was synthesized using the same procedure asdescribed for 10-(2-hydroxyethyl)-phenothiazine, (G. Cauquil in Bulletinde la Society Chemique de France, 1960, p. 1049). In the presence ofoxygen laccases (E. C. 1.10.3.2) oxidize HEPO to a HEPO radical that canbe monitored photometrically at 528 nm.

The Coprinus cinereus laccase and the Polyporus pinsitus laccase weremeasured using 0.4 mM HEPO in 50 mM MES-NaOH, pH 5.5. The absorbance at528 nm was followed for 200 s and the rate calculated from the linearpart of the progress curve.

The Myceliophthora thermophila laccase was measured using 0.4 mM HEPO in25 mM Tris-HCl, pH 7.5, 0.05% Tween-20 at 30° C. The absorbance at 528nm was followed for 200 s and the rate calculated from the linear partof the progress curve.

Expression of Laccase Variants

According to the invention, a DNA sequence encoding the variant producedby methods described above, or by any alternative methods known in theart, can be expressed, in enzyme form, using an expression vector whichtypically includes control sequences encoding a promoter, operator,ribosome binding site, translation initiation signal, and, optionally, arepressor gene or various activator genes.

The recombinant expression vector carrying the DNA sequence encoding alaccase variant of the invention may be any vector which mayconveniently be subjected to recombinant DNA procedures, and the choiceof vector will often depend on the host cell into which it is to beintroduced. Thus, the vector may be an autonomously replicating vector,i.e. a vector which exists as an extrachromosomal entity, thereplication of which is independent of chromosomal replication, e.g. aplasmid, a bacteriophage or an extrachromosomal element, minichromosomeor an artificial chromosome. Alternatively, the vector may be one which,when introduced into a host cell, is integrated into the host cellgenome and replicated together with the chromosome(s) into which it hasbeen integrated.

In the vector, the DNA sequence should be operably connected to asuitable promoter sequence. The promoter may be any DNA sequence whichshows transcriptional activity in the host cell of choice and may bederived from genes encoding proteins either homologous or heterologousto the host cell. Examples of suitable promoters for directing thetranscription of the DNA sequence encoding a laccase variant of theinvention, especially in a fungal host, are those derived from the geneencoding A. oryzae TAKA amylase, Rhizomucor miehei aspartic proteinase,A. niger neutral α-amylase, A. niger acid stable α-amylase, A. nigerglucoamylase, Rhizomucor miehei lipase, A. oryzae alkaline protease, A.oryzae triose phosphate isomerase or A. nidulans acetamidase.

The expression vector of the invention may also comprise a suitabletranscription terminator and, in eukaryotes, polyadenylation sequencesoperably connected to the DNA sequence encoding the laccase variant ofthe invention. Termination and polyadenylation sequences may suitably bederived from the same sources as the promoter.

The vector may further comprise a DNA sequence enabling the vector toreplicate in the host cell in question. Examples of such sequences arethe origins of replication of plasmids pUC19, pACYC177, pUB110, pE194,pAMB1 and pIJ702.

The vector may also comprise a selectable marker, e.g. a gene, theproduct of which complements a defect in the host cell, such as onewhich confers antibiotic resistance such as ampicillin, kanamycin,chloramphenicol or tetracyclin resistance. Furthermore, the vector maycomprise Aspergillus selection markers such as amdS, argB, niaD and sC,a marker giving rise to hygromycin resistance, or the selection may beaccomplished by co-transformation, e.g. as described in WO 91/17243.

The procedures used to ligate the DNA construct of the inventionencoding a laccase variant, the promoter, terminator and other elements,respectively, and to insert them into suitable vectors containing theinformation necessary for replication, are well known to persons skilledin the art (cf., for instance, Sambrook et al. (1989)).

The cell of the invention, either comprising a DNA construct or anexpression vector of the invention as defined above, is advantageouslyused as a host cell in the recombinant production of a laccase variantof the invention. The cell may be transformed with the DNA construct ofthe invention encoding the variant, conveniently by integrating the DNAconstruct (in one or more copies) in the host chromosome. Thisintegration is generally considered to be an advantage as the DNAsequence is more likely to be stably maintained in the cell. Integrationof the DNA constructs into the host chromosome may be performedaccording to conventional methods, e.g. by homologous or heterologousrecombination. Alternatively, the cell may be transformed with anexpression vector as described above in connection with the differenttypes of host cells.

The cell of the invention may be a cell of a higher organism such as amammal or an insect, but is preferably a microbial cell, e.g. a fungalcell.

The filamentous fungus may advantageously belong to a species ofAspergillus, e.g. Aspergillus oryzae or Aspergillus niger. Fungal cellsmay be transformed by a process involving protoplast formation andtransformation of the protoplasts followed by regeneration of the cellwall in a manner known per se. A suitable procedure for transformationof Aspergillus host cells is described in EP 238 023.

In a yet further aspect, the present invention relates to a method ofproducing a laccase variant of the invention, which method comprisescultivating a host cell as described above under conditions conducive tothe production of the variant and recovering the variant from the cellsand/or culture medium.

The medium used to cultivate the cells may be any conventional mediumsuitable for growing the host cell in question and obtaining expressionof the laccase variant of the invention. Suitable media are availablefrom commercial suppliers or may be prepared according to publishedrecipes (e.g. as described in catalogues of the American Type CultureCollection)

The laccase variant secreted from the host cells may conveniently berecovered from the culture medium by well-known procedures, includingseparating the cells from the medium by centrifugation or filtration,and precipitating proteinaceous components of the medium by means of asalt such as ammonium sulphate, followed by the use of chromatographicprocedures such as ion exchange chromatography, affinity chromatography,or the like.

Industrial Applications

The laccase variants of this invention possesses valuable propertiesallowing for various industrial applications, in particular ligninmodification, paper strengthening, dye transfer inhibition indetergents, phenol polymerization, hair dyeing, textile dyeing,bleaching of textiles (in particular bleaching of denim as described inWO 96/12845 and WO 96/12846) and waste water treatment.

A detergent additive comprising a laccase variant of the presentinvention may be in the form of a non-dusting granulate, a stabilizedliquid or a protected enzyme. This detergent additive may furthercomprise one or more other enzymes, such as a protease, a lipase, anamylase and/or a cellulase. A detergent composition comprising a laccasevariant of the present invention may further comprise a surfactant. Thisdetergent composition may additionally comprise one or more otherenzymes, such as a protease, a lipase, an amylase and/or a cellulase.

                                      APPENDIX 1                                  __________________________________________________________________________    SEQRES                                                                              1  A  504                                                                              GLN ILE VAL ASN SER VAL ASP THR MET THR LEU THR ASN                            SEQRES 2 A 504 ALA ASN VAL SER PRO ASP GLY PHE THR ARG                       ALA GLY ILE                                                      SEQRES 3 A 504 LEU VAL ASN GLY VAL HIS GLY PRO LEU ILE ARG GLY GLY                          SEQRES 4 A 504 LYS ASN ASP ASN PHE GLU LEU ASN VAL VAL                       ASN ASP LEU                                                      SEQRES 5 A 504 ASP ASN PRO THR MET LEU ARG PRO THR SER ILE HIS TRP                          SEQRES 6 A 504 HIS GLY LEU PHE GLN ARG GLY THR ASN TRP                       ALA ASN GLY                                                      SEQRES 7 A 504 ALA ASP GLY VAL ASN GLN CYS PRO ILE SER PRO GLY HIS                          SEQRES 8 A 504 ALA PHE LEU TYR LYS PHE THR PRO ALA GLY                       HIS ALA GLY                                                      SEQRES 9 A 504 THR PHE TRP TYR HIS SER HIS PHE GLY THR GLN TYR CYS                          SEQRES 10 A 504 ASP GLY LEU ARG GLY PRO MET VAL ILE TYR                      ASP ASP ASN                                                      SEQRES 11 A 504 ASP PRO HIS ALA ALA LEU TYR ASP GLU ASP ASP GLU ASN                         SEQRES 12 A 504 THR ILE ILE THR LEU ALA ASP TRP TYR HIS                      ILE PRO ALA                                                      SEQRES 13 A 504 PRO SER ILE GLN GLY ALA ALA GLN PRO ASP ALA THR LEU                         SEQRES 14 A 504 ILE ASN GLY LYS GLY ARG TYR VAL GLY GLY                      PRO ALA ALA                                                      SEQRES 15 A 504 GLU LEU SER ILE VAL ASN VAL GLU GLN GLY LYS LYS TYR                         SEQRES 16 A 504 ARG MET ARG LEU ILE SER LEU SER CYS ASP                      PRO ASN TRP                                                      SEQRES 17 A 504 GLN PHE SER ILE ASP GLY HIS GLU LEU THR ILE ILE GLU                         SEQRES 18 A 504 VAL ASP GLY ASN LEU THR GLU PRO HIS THR                      VAL ASP ARG                                                      SEQRES 19 A 504 LEU GLN ILE PHE THR GLY GLN ARG TYR SER PHE VAL LEU                         SEQRES 20 A 504 ASP ALA ASN GLN PRO VAL ASP ASN TYR TRP                      ILE ARG ALA                                                      SEQRES 21 A 504 GLN PRO ASN LYS GLY ARG ASN GLY LEU ALA GLY THR PHE                         SEQRES 22 A 504 ALA ASN GLY VAL ASN SER ALA ILE LEU ARG                      TYR ALA GLY                                                      SEQRES 23 A 504 ALA ALA ASN ALA ASP PRO THR THR SER ALA ASN PRO ASN                         SEQRES 24 A 504 PRO ALA GLN LEU ASN GLU ALA ASP LEU HIS                      ALA LEU ILE                                                      SEQRES 25 A 504 ASP PRO ALA ALA PRO GLY ILE PRO THR PRO GLY ALA ALA                         SEQRES 26 A 504 ASN VAL ASN LEU ARG PHE GLN LEU GLY PHE                      SER GLY GLY                                                      SEQRES 27 A 504 ARG PHE THR ILE ASN GLY THR ALA TYR GLU SER PRO SER                         SEQRES 28 A 504 VAL PRO THR LEU LEU GLN ILE MET SER GLY                      ALA GLN SER                                                      SEQRES 29 A 504 ALA ASN ASP LEU LEU PRO ALA GLY SER VAL TYR GLU LEU                         SEQRES 30 A 504 PRO ARG ASN GLN VAL VAL GLU LEU VAL VAL                      PRO ALA GLY                                                      SEQRES 31 A 504 VAL LEU GLY GLY PRO HIS PRO PHE HIS LEU HIS GLY HIS                         SEQRES 32 A 504 ALA PHE SER VAL VAL ARG SER ALA GLY SER                      SER THR TYR                                                      SEQRES 33 A 504 ASN PHE VAL ASN PRO VAL LYS ARG ASP VAL VAL SER LEU                         SEQRES 34 A 504 GLY VAL THR GLY ASP GLU VAL THR ILE ARG                      PHE VAL THR                                                      SEQRES 35 A 504 ASP ASN PRO GLY PRO TRP PHE PHE HIS CYS HIS ILE GLU                         SEQRES 36 A 504 PHE HIS LEU MET ASN GLY LEU ALA ILE VAL                      PHE ALA GLU                                                      SEQRES 37 A 504 ASP MET ALA ASN THR VAL ASP ALA ASN ASN PRO PRO VAL                         SEQRES 38 A 504 GLU TRP ALA GLN LEU CYS GLU ILE TYR ASP                      ASP LEU PRO                                                      SEQRES 39 A 504 PRO GLU ALA THR SER ILE GLN THR VAL VAL                     SSBOND                                                                              1 CYS                                                                             85                                                                              CYS                                                                             487                                                               SSBOND 2 CYS 117 CYS 204                                                    CRYST 45.390                                                                            85.720                                                                            143.070                                                                            90.00                                                                             90.00                                                                             90.00                                                                             P212121                                        SCALE1  0.02203                                                                            0.00000                                                                            0.00000                                                                            0.00000                                                  SCALE2 0.00000 0.01167 0.00000 0.00000                                        SCALE3 0.00000 0.00000 0.00699 0.00000                                      ATOM 1   N   ALA A  1   0  18.748                                                                            34.495                                                                            5.326                                                                             1.00                                                                              36.36                                ATOM 2 CA ALA A 1 0 19.554 35.757 5.185 1.00 35.87                            ATOM 3 C ALA A 1 0 19.785 36.380 6.558 1.00 34.53                             ATOM 4 O ALA A 1 0 19.248 35.884 7.577 1.00 35.40                             ATOM 5 CB ALA A 1 0 19.050 36.675 4.107 1.00 36.65                            ATOM 6 N ILE A 2 0 20.844 37.201 6.659 1.00 31.00                             ATOM 7 CA ILE A 2 0 21.310 37.654 7.963 1.00 27.71                            ATOM 8 C ILE A 2 0 21.368 39.165 8.117 1.00 25.19                             ATOM 9 O ILE A 2 0 21.789 39.861 7.192 1.00 23.77                             ATOM 10 CB ILE A 2 0 22.744 37.107 8.206 1.00 28.28                           ATOM 11 CG1 ILE A 2 0 22.790 35.590 8.022 1.00 28.54                          ATOM 12 CG2 ILE A 2 0 23.285 37.557 9.554 1.00 27.91                          ATOM 13 CD1 ILE A 2 0 23.334 34.738 9.130 1.00 29.32                          ATOM 14 N VAL A 3 0 20.986 39.659 9.283 1.00 22.31                            ATOM 15 CA VAL A 3 0 21.093 41.092 9.540 1.00 22.78                           ATOM 16 C VAL A 3 0 22.246 41.297 10.524 1.00 22.62                           ATOM 17 O VAL A 3 0 22.460 40.556 11.467 1.00 21.74                           ATOM 18 CB VAL A 3 0 19.801 41.849 9.799 1.00 23.54                           ATOM 19 CG1 VAL A 3 0 18.537 40.985 9.684 1.00 21.30                          ATOM 20 CG2 VAL A 3 0 19.760 42.709 11.055 1.00 21.32                         ATOM 21 N ASN A 4 0 23.122 42.261 10.209 1.00 23.39                           ATOM 22 CA ASN A 4 0 24.303 42.520 11.021 1.00 23.45                          ATOM 23 C ASN A 4 0 24.002 43.517 12.126 1.00 24.44                           ATOM 24 O ASN A 4 0 22.928 44.122 12.160 1.00 23.05                           ATOM 25 CB ASN A 4 0 25.477 42.965 10.149 1.00 24.77                          ATOM 26 CG ASN A 4 0 25.726 41.991 9.021 1.00 26.62                           ATOM 27 OD1 ASN A 4 0 25.668 42.388 7.849 1.00 30.29                          ATOM 28 ND2 ASN A 4 0 25.923 40.719 9.324 1.00 27.59                          ATOM 29 N SER A 5 0 24.960 43.707 13.040 1.00 24.28                           ATOM 30 CA SER A 5 0 24.702 44.636 14.143 1.00 25.77                          ATOM 31 C SER A 5 0 24.595 46.090 13.701 1.00 24.41                           ATOM 32 O SER A 5 0 23.973 46.862 14.452 1.00 23.55                           ATOM 33 CB SER A 5 0 25.741 44.405 15.240 1.00 26.18                          ATOM 34 OG SER A 5 0 26.976 44.750 14.641 1.00 27.89                          ATOM 35 N VAL A 6 0 25.104 46.517 12.539 1.00 24.01                           ATOM 36 CA VAL A 6 0 24.770 47.863 12.096 1.00 25.06                          ATOM 37 C VAL A 6 0 24.131 47.617 10.731 1.00 25.57                           ATOM 38 O VAL A 6 0 24.778 47.030 9.874 1.00 28.07                            ATOM 39 CB VAL A 6 0 25.722 49.032 12.155 1.00 26.65                          ATOM 40 CG1 VAL A 6 0 26.937 48.759 13.025 1.00 26.73                         ATOM 41 CG2 VAL A 6 0 26.098 49.614 10.801 1.00 25.50                         ATOM 42 N ASP A 7 0 22.848 47.952 10.605 1.00 23.82                           ATOM 43 CA ASP A 7 0 22.173 47.543 9.369 1.00 24.07                           ATOM 44 C ASP A 7 0 20.794 48.170 9.276 1.00 23.66                            ATOM 45 O ASP A 7 0 20.342 48.845 10.204 1.00 23.47                           ATOM 46 CB ASP A 7 0 21.996 46.012 9.444 1.00 23.43                           ATOM 47 CG ASP A 7 0 22.017 45.317 8.111 1.00 23.78                           ATOM 48 OD1 ASP A 7 0 21.805 45.937 7.055 1.00 23.74                          ATOM 49 OD2 ASP A 7 0 22.255 44.089 8.099 1.00 24.62                          ATOM 50 N THR A 8 0 20.155 47.881 8.158 1.00 23.88                            ATOM 51 CA THR A 8 0 18.799 48.359 7.928 1.00 24.45                           ATOM 52 C THR A 8 0 17.813 47.189 7.950 1.00 22.49                            ATOM 53 O THR A 8 0 18.143 46.142 7.377 1.00 22.56                            ATOM 54 CB THR A 8 0 18.694 49.108 6.579 1.00 25.75                           ATOM 55 OG1 THR A 8 0 19.573 50.242 6.719 1.00 28.53                          ATOM 56 CG2 THR A 8 0 17.295 49.656 6.339 1.00 25.55                          ATOM 57 N MET A 9 0 16.677 47.364 8.602 1.00 19.10                            ATOM 58 CA MET A 9 0 15.650 46.311 8.616 1.00 20.47                           ATOM 59 C MET A 9 0 14.392 46.863 7.925 1.00 21.97                            ATOM 60 O MET A 9 0 13.638 47.638 8.544 1.00 19.49                            ATOM 61 CB MET A 9 0 15.308 45.871 10.022 1.00 20.49                          ATOM 62 CG MET A 9 0 16.351 44.982 10.682 1.00 22.11                          ATOM 63 SD MET A 9 0 16.192 44.917 12.482 1.00 24.71                          ATOM 64 CE MET A 9 0 14.640 44.024 12.635 1.00 22.61                          ATOM 65 N THR A 10 0 14.246 46.516 6.641 1.00 21.81                           ATOM 66 CA THR A 10 0 13.073 47.064 5.926 1.00 23.43                          ATOM 67 C THR A 10 0 11.912 46.081 6.046 1.00 22.90                           ATOM 68 O THR A 10 0 12.056 44.890 5.719 1.00 23.55                           ATOM 69 CB THR A 10 0 13.390 47.384 4.459 1.00 24.69                          ATOM 70 OG1 THR A 10 0 14.533 48.261 4.456 1.00 26.08                         ATOM 71 CG2 THR A 10 0 12.216 48.028 3.742 1.00 23.95                         ATOM 72 N LEU A 11 0 10.820 46.600 6.583 1.00 21.13                           ATOM 73 CA LEU A 11 0 9.615 45.836 6.846 1.00 21.10                           ATOM 74 C LEU A 11 0 8.607 45.957 5.709 1.00 24.58                            ATOM 75 O LEU A 11 0 8.124 47.056 5.358 1.00 23.89                            ATOM 76 CB LEU A 11 0 9.045 46.411 8.129 1.00 21.29                           ATOM 77 CG LEU A 11 0 9.474 45.955 9.508 1.00 22.26                           ATOM 78 CD1 LEU A 11 0 10.952 45.742 9.692 1.00 22.42                         ATOM 79 CD2 LEU A 11 0 8.978 46.931 10.583 1.00 22.75                         ATOM 80 N THR A 12 0 8.272 44.836 5.057 1.00 24.01                            ATOM 81 CA THR A 12 0 7.302 44.851 3.980 1.00 24.33                           ATOM 82 C THR A 12 0 6.322 43.677 4.123 1.00 25.34                            ATOM 83 O THR A 12 0 6.480 42.740 4.913 1.00 25.62                            ATOM 84 CB THR A 12 0 7.882 44.776 2.560 1.00 25.12                           ATOM 85 OG1 THR A 12 0 8.575 43.548 2.377 1.00 24.05                          ATOM 86 CG2 THR A 12 0 8.847 45.905 2.217 1.00 25.26                          ATOM 87 N ASN A 13 0 5.261 43.760 3.335 1.00 24.09                            ATOM 88 CA ASN A 13 0 4.232 42.722 3.299 1.00 22.87                           ATOM 89 C ASN A 13 0 4.422 41.954 1.989 1.00 22.13                            ATOM 90 O ASN A 13 0 4.809 42.600 1.023 1.00 22.32                            ATOM 91 CB ASN A 13 0 2.852 43.355 3.311 1.00 21.58                           ATOM 92 CG ASN A 13 0 2.526 44.060 4.607 1.00 22.50                           ATOM 93 OD1 ASN A 13 0 2.187 45.245 4.648 1.00 22.20                          ATOM 94 ND2 ASN A 13 0 2.615 43.306 5.705 1.00 21.81                          ATOM 95 N ALA A 14 0 4.218 40.655 1.985 1.00 21.00                            ATOM 96 CA ALA A 14 0 4.270 39.869 0.762 1.00 21.93                           ATOM 97 C ALA A 14 0 3.571 38.533 1.078 1.00 20.77                            ATOM 98 O ALA A 14 0 3.292 38.309 2.259 1.00 20.45                            ATOM 99 CB ALA A 14 0 5.676 39.618 0.248 1.00 23.72                           ATOM 100 N ASN A 15 0 3.366 37.695 0.072 1.00 18.88                           ATOM 101 CA ASN A 15 0 2.748 36.412 0.337 1.00 19.67                          ATOM 102 C ASN A 15 0 3.798 35.457 0.873 1.00 19.19                           ATOM 103 O ASN A 15 0 4.891 35.474 0.338 1.00 19.57                           ATOM 104 CB ASN A 15 0 2.114 35.721 -0.875 1.00 21.13                         ATOM 105 CG ASN A 15 0 0.839 36.457 -1.284 1.00 21.15                         ATOM 106 OD1 ASN A 15 0 0.343 37.207 -0.472 1.00 20.87                        ATOM 107 ND2 ASN A 15 0 0.379 36.284 -2.501 1.00 20.00                        ATOM 108 N VAL A 16 0 3.358 34.614 1.772 1.00 19.11                           ATOM 109 CA VAL A 16 0 4.322 33.628 2.342 1.00 18.90                          ATOM 110 C VAL A 16 0 3.626 32.293 2.345 1.00 19.25                           ATOM 111 O VAL A 16 0 2.386 32.281 2.406 1.00 15.71                           ATOM 112 CB VAL A 16 0 4.612 34.317 3.691 1.00 19.95                          ATOM 113 CG1 VAL A 16 0 3.990 33.749 4.937 1.00 18.58                         ATOM 114 CG2 VAL A 16 0 6.091 34.603 3.814 1.00 21.38                         ATOM 115 N SER A 17 0 4.312 31.157 2.303 1.00 18.57                           ATOM 116 CA SER A 17 0 3.678 29.869 2.410 1.00 20.90                          ATOM 117 C SER A 17 0 4.608 28.866 3.065 1.00 21.12                           ATOM 118 O SER A 17 0 5.106 27.939 2.448 1.00 21.24                           ATOM 119 CB SER A 17 0 3.186 29.285 1.080 1.00 23.95                          ATOM 120 OG SER A 17 0 4.204 29.399 0.125 1.00 26.79                          ATOM 121 N PRO A 18 0 4.834 29.051 4.358 1.00 20.78                           ATOM 122 CA PRO A 18 0 5.703 28.216 5.141 1.00 20.02                          ATOM 123 C PRO A 18 0 5.197 26.793 5.376 1.00 19.74                           ATOM 124 O PRO A 18 0 5.978 25.920 5.753 1.00 17.97                           ATOM 125 CB PRO A 18 0 5.889 28.954 6.481 1.00 19.27                          ATOM 126 CG PRO A 18 0 4.701 29.832 6.536 1.00 21.41                          ATOM 127 CD PRO A 18 0 4.249 30.153 5.128 1.00 20.70                          ATOM 128 N ASP A 19 0 3.899 26.534 5.241 1.00 18.82                           ATOM 129 CA ASP A 19 0 3.323 25.227 5.475 1.00 16.87                          ATOM 130 C ASP A 19 0 2.548 24.823 4.237 1.00 17.28                           ATOM 131 O ASP A 19 0 1.713 23.929 4.337 1.00 17.84                           ATOM 132 CB ASP A 19 0 2.419 25.207 6.701 1.00 16.54                          ATOM 133 CG ASP A 19 0 1.192 26.120 6.596 1.00 16.67                          ATOM 134 OD1 ASP A 19 0 1.032 26.935 5.654 1.00 14.17                         ATOM 135 OD2 ASP A 19 0 0.360 26.045 7.529 1.00 14.56                         ATOM 136 N GLY A 20 0 2.782 25.469 3.100 1.00 17.87                           ATOM 137 CA GLY A 20 0 2.079 25.091 1.890 1.00 19.40                          ATOM 138 C GLY A 20 0 0.732 25.789 1.699 1.00 22.52                           ATOM 139 O GLY A 20 0 0.158 25.619 0.628 1.00 22.87                           ATOM 140 N PHE A 21 0 0.240 26.587 2.631 1.00 21.35                           ATOM 141 CA PHE A 21 0 -0.913 27.443 2.534 1.00 20.39                         ATOM 142 C PHE A 21 0 -0.348 28.855 2.322 1.00 21.23                          ATOM 143 O PHE A 21 0 0.475 29.316 3.122 1.00 21.26                           ATOM 144 CB PHE A 21 0 -1.742 27.472 3.814 1.00 20.80                         ATOM 145 CG PHE A 21 0 -3.059 28.180 3.695 1.00 21.91                         ATOM 146 CD1 PHE A 21 0 -3.171 29.527 3.963 1.00 22.49                        ATOM 147 CD2 PHE A 21 0 -4.207 27.470 3.327 1.00 22.51                        ATOM 148 CE1 PHE A 21 0 -4.370 30.207 3.845 1.00 22.27                        ATOM 149 CE2 PHE A 21 0 -5.419 28.128 3.203 1.00 22.79                        ATOM 150 CZ PHE A 21 0 -5.498 29.497 3.474 1.00 23.34                         ATOM 151 N THR A 22 0 -0.638 29.514 1.225 1.00 20.20                          ATOM 152 CA THR A 22 0 -0.143 30.850 0.977 1.00 21.36                         ATOM 153 C THR A 22 0 -1.083 31.939 1.488 1.00 21.79                          ATOM 154 O THR A 22 0 -2.271 31.952 1.162 1.00 21.19                          ATOM 155 CB THR A 22 0 0.045 31.012 -0.553 1.00 21.46                         ATOM 156 OG1 THR A 22 0 0.838 29.881 -0.934 1.00 20.09                        ATOM 157 CG2 THR A 22 0 0.693 32.353 -0.891 1.00 20.94                        ATOM 158 N ARG A 23 0 -0.562 32.871 2.257 1.00 20.80                          ATOM 159 CA ARG A 23 0 -1.230 34.008 2.844 1.00 20.78                         ATOM 160 C ARG A 23 0 -0.257 35.189 2.960 1.00 21.15                          ATOM 161 O ARG A 23 0 0.954 35.018 2.740 1.00 20.42                           ATOM 162 CB ARG A 23 0 -1.874 33.685 4.172 1.00 20.47                         ATOM 163 CG ARG A 23 0 -0.964 33.152 5.295 1.00 21.52                         ATOM 164 CD ARG A 23 0 -0.552 34.357 6.113 1.00 22.75                         ATOM 165 NE ARG A 23 0 -0.905 34.419 7.477 1.00 21.60                         ATOM 166 CZ ARG A 23 0 -0.870 35.283 8.464 1.00 19.89                         ATOM 167 NH1 ARG A 23 0 -0.526 36.565 8.453 1.00 20.19                        ATOM 168 NH2 ARG A 23 0 -1.249 34.744 9.610 1.00 18.64                        ATOM 169 N ALA A 24 0 -0.784 36.389 3.199 1.00 20.05                          ATOM 170 CA ALA A 24 0 0.140 37.541 3.243 1.00 22.03                          ATOM 171 C ALA A 24 0 0.786 37.561 4.635 1.00 21.09                           ATOM 172 O ALA A 24 0 0.200 37.124 5.637 1.00 21.16                           ATOM 173 CB ALA A 24 0 -0.578 38.836 2.902 1.00 22.98                         ATOM 174 N GLY A 25 0 2.042 37.984 4.683 1.00 20.28                           ATOM 175 CA GLY A 25 0 2.786 37.993 5.950 1.00 20.29                          ATOM 176 C GLY A 25 0 3.649 39.254 5.979 1.00 21.38                           ATOM 177 O GLY A 25 0 3.465 40.229 5.238 1.00 21.06                           ATOM 178 N ILE A 26 0 4.604 39.221 6.897 1.00 20.33                           ATOM 179 CA ILE A 26 0 5.475 40.365 7.145 1.00 20.64                          ATOM 180 C ILE A 26 0 6.903 39.886 6.932 1.00 20.00                           ATOM 181 O ILE A 26 0 7.247 38.851 7.485 1.00 21.34                           ATOM 182 CB ILE A 26 0 5.278 40.933 8.564 1.00 20.38                          ATOM 183 CG1 ILE A 26 0 3.883 41.536 8.667 1.00 20.72                         ATOM 184 CG2 ILE A 26 0 6.333 42.007 8.821 1.00 22.34                         ATOM 185 CD1 ILE A 26 0 3.310 41.822 10.024 1.00 20.76                        ATOM 186 N LEU A 27 0 7.644 40.551 6.079 1.00 19.10                           ATOM 187 CA LEU A 27 0 9.005 40.168 5.739 1.00 19.67                          ATOM 188 C LEU A 27 0 9.964 41.226 6.280 1.00 19.85                           ATOM 189 O LEU A 27 0 9.591 42.407 6.356 1.00 19.19                           ATOM 190 CB LEU A 27 0 9.138 40.172 4.219 1.00 20.26                          ATOM 191 CG LEU A 27 0 9.046 38.883 3.415 1.00 22.65                          ATOM 192 CD1 LEU A 27 0 8.127 37.835 3.989 1.00 21.10                         ATOM 193 CD2 LEU A 27 0 8.738 39.198 1.963 1.00 22.01                         ATOM 194 N VAL A 28 0 11.162 40.804 6.630 1.00 18.03                          ATOM 195 CA VAL A 28 0 12.199 41.723 7.088 1.00 17.24                         ATOM 196 C VAL A 28 0 13.289 41.573 6.040 1.00 18.99                          ATOM 197 O VAL A 28 0 13.791 40.453 5.863 1.00 20.36                          ATOM 198 CB VAL A 28 0 12.762 41.415 8.491 1.00 16.50                         ATOM 199 CG1 VAL A 28 0 13.899 42.361 8.845 1.00 15.41                        ATOM 200 CG2 VAL A 28 0 11.681 41.517 9.558 1.00 15.42                        ATOM 201 N ASN A 29 0 13.575 42.601 5.256 1.00 20.78                          ATOM 202 CA ASN A 29 0 14.567 42.579 4.198 1.00 20.46                         ATOM 203 C ASN A 29 0 14.316 41.435 3.226 1.00 23.05                          ATOM 204 O ASN A 29 0 15.247 40.675 2.880 1.00 23.62                          ATOM 205 CB ASN A 29 0 15.982 42.446 4.764 1.00 21.06                         ATOM 206 CG ASN A 29 0 16.475 43.654 5.522 1.00 22.44                         ATOM 207 OD1 ASN A 29 0 15.870 44.722 5.434 1.00 23.47                        ATOM 208 ND2 ASN A 29 0 17.560 43.507 6.288 1.00 22.23                        ATOM 209 N GLY A 30 0 13.053 41.215 2.878 1.00 23.18                          ATOM 210 CA GLY A 30 0 12.662 40.181 1.922 1.00 23.36                         ATOM 211 C GLY A 30 0 12.723 38.757 2.436 1.00 23.85                          ATOM 212 O GLY A 30 0 12.707 37.814 1.633 1.00 25.17                          ATOM 213 N VAL A 31 0 12.832 38.585 3.755 1.00 21.85                          ATOM 214 CA VAL A 31 0 12.999 37.276 4.352 1.00 20.55                         ATOM 215 C VAL A 31 0 12.031 37.190 5.548 1.00 19.91                          ATOM 216 O VAL A 31 0 11.796 38.172 6.269 1.00 17.50                          ATOM 217 CB VAL A 31 0 14.436 37.020 4.856 1.00 21.36                         ATOM 218 CG1 VAL A 31 0 14.556 35.709 5.626 1.00 20.79                        ATOM 219 CG2 VAL A 31 0 15.495 37.005 3.757 1.00 21.84                        ATOM 220 N HIS A 32 0 11.489 35.984 5.698 1.00 17.05                          ATOM 221 CA HIS A 32 0 10.592 35.729 6.797 1.00 18.61                         ATOM 222 C HIS A 32 0 11.417 35.499 8.050 1.00 17.67                          ATOM 223 O HIS A 32 0 11.873 34.385 8.216 1.00 18.72                          ATOM 224 CB HIS A 32 0 9.676 34.543 6.493 1.00 21.00                          ATOM 225 CG HIS A 32 0 8.639 34.208 7.517 1.00 23.80                          ATOM 226 ND1 HIS A 32 0 7.744 33.174 7.332 1.00 25.14                         ATOM 227 CD2 HIS A 32 0 8.331 34.720 8.735 1.00 25.32                         ATOM 228 CE1 HIS A 32 0 6.942 33.061 8.385 1.00 25.36                         ATOM 229 NE2 HIS A 32 0 7.271 33.986 9.260 1.00 26.23                         ATOM 230 N GLY A 33 0 11.522 36.446 8.960 1.00 16.23                          ATOM 231 CA GLY A 33 0 12.276 36.252 10.198 1.00 16.97                        ATOM 232 C GLY A 33 0 13.740 35.869 10.083 1.00 15.54                         ATOM 233 O GLY A 33 0 14.228 34.885 10.609 1.00 15.13                         ATOM 234 N PRO A 34 0 14.555 36.734 9.475 1.00 15.75                          ATOM 235 CA PRO A 34 0 16.012 36.561 9.359 1.00 14.70                         ATOM 236 C PRO A 34 0 16.734 36.660 10.701 1.00 14.02                         ATOM 237 O PRO A 34 0 16.241 37.252 11.673 1.00 10.44                         ATOM 238 CB PRO A 34 0 16.491 37.699 8.435 1.00 14.40                         ATOM 239 CG PRO A 34 0 15.441 38.742 8.783 1.00 15.11                         ATOM 240 CD PRO A 34 0 14.113 38.005 8.905 1.00 13.69                         ATOM 241 N LEU A 35 0 17.925 36.049 10.767 1.00 13.60                         ATOM 242 CA LEU A 35 0 18.748 36.022 11.963 1.00 14.35                        ATOM 243 C LEU A 35 0 19.462 37.359 12.161 1.00 16.25                         ATOM 244 O LEU A 35 0 20.015 37.902 11.210 1.00 14.10                         ATOM 245 CB LEU A 35 0 19.834 34.916 11.862 1.00 15.33                        ATOM 246 CG LEU A 35 0 20.958 34.943 12.911 1.00 17.74                        ATOM 247 CD1 LEU A 35 0 20.486 34.698 14.348 1.00 16.30                       ATOM 248 CD2 LEU A 35 0 22.052 33.934 12.575 1.00 16.60                       ATOM 249 N ILE A 36 0 19.471 37.855 13.384 1.00 16.71                         ATOM 250 CA ILE A 36 0 20.265 39.027 13.738 1.00 16.66                        ATOM 251 C ILE A 36 0 21.403 38.487 14.620 1.00 17.92                         ATOM 252 O ILE A 36 0 21.183 37.732 15.573 1.00 17.20                         ATOM 253 CB ILE A 36 0 19.560 40.129 14.533 1.00 16.60                        ATOM 254 CG1 ILE A 36 0 18.389 40.771 13.771 1.00 16.09                       ATOM 255 CG2 ILE A 36 0 20.565 41.226 14.917 1.00 17.67                       ATOM 256 CD1 ILE A 36 0 17.590 41.754 14.629 1.00 15.88                       ATOM 257 N ARG A 37 0 22.647 38.829 14.288 1.00 18.72                         ATOM 258 CA ARG A 37 0 23.754 38.315 15.091 1.00 19.94                        ATOM 259 C ARG A 37 0 24.839 39.369 15.280 1.00 20.08                         ATOM 260 O ARG A 37 0 24.979 40.249 14.450 1.00 20.52                         ATOM 261 CB ARG A 37 0 24.395 37.077 14.465 1.00 21.72                        ATOM 262 CG ARG A 37 0 25.102 37.393 13.171 1.00 24.46                        ATOM 263 CD ARG A 37 0 26.113 36.339 12.762 1.00 26.90                        ATOM 264 NE ARG A 37 0 26.584 36.571 11.381 1.00 29.30                        ATOM 265 CZ ARG A 37 0 26.838 35.571 10.528 1.00 31.29                        ATOM 266 NH1 ARG A 37 0 26.711 34.283 10.851 1.00 31.37                       ATOM 267 NH2 ARG A 37 0 27.252 35.827 9.291 1.00 31.66                        ATOM 268 N GLY A 38 0 25.587 39.223 16.361 1.00 20.22                         ATOM 269 CA GLY A 38 0 26.716 40.121 16.611 1.00 18.98                        ATOM 270 C GLY A 38 0 27.533 39.545 17.765 1.00 18.08                         ATOM 271 O GLY A 38 0 27.259 38.421 18.225 1.00 15.92                         ATOM 272 N GLY A 39 0 28.436 40.412 18.238 1.00 17.65                         ATOM 273 CA GLY A 39 0 29.322 40.026 19.351 1.00 16.23                        ATOM 274 C GLY A 39 0 28.861 40.774 20.592 1.00 17.21                         ATOM 275 O GLY A 39 0 28.157 41.784 20.489 1.00 17.27                         ATOM 276 N LYS A 40 0 29.276 40.328 21.764 1.00 16.58                         ATOM 277 CA LYS A 40 0 28.839 40.805 23.057 1.00 18.03                        ATOM 278 C LYS A 40 0 29.185 42.267 23.348 1.00 20.44                         ATOM 279 O LYS A 40 0 28.562 42.878 24.221 1.00 19.42                         ATOM 280 CB LYS A 40 0 29.394 39.933 24.185 1.00 16.74                        ATOM 281 CG LYS A 40 0 30.892 39.997 24.370 1.00 17.98                        ATOM 282 CD LYS A 40 0 31.333 39.170 25.569 1.00 20.66                        ATOM 283 CE LYS A 40 0 32.809 38.768 25.493 1.00 21.70                        ATOM 284 NZ LYS A 40 0 33.227 38.111 26.757 1.00 23.11                        ATOM 285 N ASN A 41 0 30.181 42.780 22.645 1.00 21.43                         ATOM 286 CA ASN A 41 0 30.536 44.171 22.840 1.00 25.14                        ATOM 287 C ASN A 41 0 30.092 44.976 21.644 1.00 24.05                         ATOM 288 O ASN A 41 0 30.409 46.161 21.655 1.00 25.66                         ATOM 289 CB ASN A 41 0 32.052 44.326 23.111 1.00 27.02                        ATOM 290 CG ASN A 41 0 32.434 43.606 24.404 1.00 29.76                        ATOM 291 OD1 ASN A 41 0 33.398 42.832 24.431 1.00 31.54                       ATOM 292 ND2 ASN A 41 0 31.663 43.825 25.473 1.00 30.13                       ATOM 293 N ASP A 42 0 29.424 44.447 20.631 1.00 23.80                         ATOM 294 CA ASP A 42 0 29.073 45.325 19.506 1.00 24.12                        ATOM 295 C ASP A 42 0 28.169 46.484 19.891 1.00 24.24                         ATOM 296 O ASP A 42 0 27.420 46.428 20.872 1.00 22.42                         ATOM 297 CB ASP A 42 0 28.388 44.528 18.392 1.00 26.65                        ATOM 298 CG ASP A 42 0 29.404 43.599 17.773 1.00 28.94                        ATOM 299 OD1 ASP A 42 0 30.603 43.754 18.056 1.00 31.45                       ATOM 300 OD2 ASP A 42 0 29.026 42.708 17.009 1.00 31.69                       ATOM 301 N ASN A 43 0 28.258 47.547 19.090 1.00 24.72                         ATOM 302 CA ASN A 43 0 27.316 48.660 19.255 1.00 26.50                        ATOM 303 C ASN A 43 0 26.293 48.430 18.128 1.00 26.23                         ATOM 304 O ASN A 43 0 26.723 48.420 16.979 1.00 25.02                         ATOM 305 CB ASN A 43 0 27.934 50.047 19.128 1.00 28.45                        ATOM 306 CG ASN A 43 0 28.858 50.244 20.323 1.00 31.09                        ATOM 307 OD1 ASN A 43 0 30.041 50.502 20.106 1.00 33.11                       ATOM 308 ND2 ASN A 43 0 28.364 50.055 21.531 1.00 31.18                       ATOM 309 N PHE A 44 0 25.039 48.155 18.468 1.00 24.63                         ATOM 310 CA PHE A 44 0 24.083 47.897 17.393 1.00 23.28                        ATOM 311 C PHE A 44 0 23.450 49.191 16.916 1.00 22.36                         ATOM 312 O PHE A 44 0 23.024 50.008 17.735 1.00 21.07                         ATOM 313 CB PHE A 44 0 22.959 46.965 17.853 1.00 22.04                        ATOM 314 CG PHE A 44 0 23.376 45.525 17.955 1.00 22.96                        ATOM 315 CD1 PHE A 44 0 22.779 44.562 17.153 1.00 23.91                       ATOM 316 CD2 PHE A 44 0 24.330 45.120 18.869 1.00 22.03                       ATOM 317 CE1 PHE A 44 0 23.131 43.230 17.253 1.00 24.42                       ATOM 318 CE2 PHE A 44 0 24.689 43.797 18.974 1.00 23.25                       ATOM 319 CZ PHE A 44 0 24.095 42.837 18.168 1.00 24.02                        ATOM 320 N GLU A 45 0 23.350 49.343 15.604 1.00 22.78                         ATOM 321 CA GLU A 45 0 22.611 50.482 15.054 1.00 24.47                        ATOM 322 C GLU A 45 0 21.619 49.884 14.055 1.00 23.79                         ATOM 323 O GLU A 45 0 22.017 49.587 12.924 1.00 24.40                         ATOM 324 CB GLU A 45 0 23.543 51.473 14.368 1.00 27.07                        ATOM 325 CG GLU A 45 0 24.474 52.130 15.374 1.00 31.60                        ATOM 326 CD GLU A 45 0 25.380 53.179 14.772 1.00 33.90                        ATOM 327 OE1 GLU A 45 0 25.354 53.438 13.559 1.00 35.62                       ATOM 328 OE2 GLU A 45 0 26.155 53.748 15.565 1.00 36.42                       ATOM 329 N LEU A 46 0 20.369 49.684 14.465 1.00 22.18                         ATOM 330 CA LEU A 46 0 19.419 49.044 13.556 1.00 21.22                        ATOM 331 C LEU A 46 0 18.348 50.001 13.077 1.00 21.27                         ATOM 332 O LEU A 46 0 17.464 50.429 13.812 1.00 21.60                         ATOM 333 CB LEU A 46 0 18.837 47.811 14.262 1.00 20.72                        ATOM 334 CG LEU A 46 0 19.827 46.658 14.403 1.00 21.28                        ATOM 335 CD1 LEU A 46 0 19.334 45.621 15.397 1.00 20.83                       ATOM 336 CD2 LEU A 46 0 20.148 46.034 13.052 1.00 18.33                       ATOM 337 N ASN A 47 0 18.438 50.403 11.823 1.00 21.09                         ATOM 338 CA ASN A 47 0 17.498 51.344 11.252 1.00 22.37                        ATOM 339 C ASN A 47 0 16.273 50.558 10.803 1.00 22.18                         ATOM 340 O ASN A 47 0 16.390 49.810 9.847 1.00 23.41                          ATOM 341 CB ASN A 47 0 18.131 52.104 10.066 1.00 24.01                        ATOM 342 CG ASN A 47 0 17.226 53.243 9.615 1.00 25.54                         ATOM 343 OD1 ASN A 47 0 16.443 53.772 10.413 1.00 26.53                       ATOM 344 ND2 ASN A 47 0 17.332 53.612 8.346 1.00 26.01                        ATOM 345 N VAL A 48 0 15.147 50.692 11.475 1.00 22.04                         ATOM 346 CA VAL A 48 0 13.918 49.995 11.140 1.00 21.99                        ATOM 347 C VAL A 48 0 13.026 50.879 10.269 1.00 21.82                         ATOM 348 O VAL A 48 0 12.532 51.910 10.699 1.00 20.61                         ATOM 349 CB VAL A 48 0 13.176 49.579 12.430 1.00 22.64                        ATOM 350 CG1 VAL A 48 0 11.819 48.931 12.148 1.00 21.99                       ATOM 351 CG2 VAL A 48 0 14.098 48.631 13.216 1.00 21.68                       ATOM 352 N VAL A 49 0 12.931 50.512 9.009 1.00 21.79                          ATOM 353 CA VAL A 49 0 12.164 51.167 7.966 1.00 21.34                         ATOM 354 C VAL A 49 0 10.816 50.460 7.795 1.00 21.12                          ATOM 355 O VAL A 49 0 10.703 49.308 7.365 1.00 19.76                          ATOM 356 CB VAL A 49 0 12.983 51.189 6.665 1.00 22.02                         ATOM 357 CG1 VAL A 49 0 12.267 51.913 5.519 1.00 21.70                        ATOM 358 CG2 VAL A 49 0 14.312 51.933 6.906 1.00 21.47                        ATOM 359 N ASN A 50 0 9.767 51.112 8.257 1.00 20.26                           ATOM 360 CA ASN A 50 0 8.424 50.611 8.215 1.00 22.70                          ATOM 361 C ASN A 50 0 7.751 50.899 6.869 1.00 25.99                           ATOM 362 O ASN A 50 0 7.043 51.925 6.735 1.00 27.06                           ATOM 363 CB ASN A 50 0 7.549 51.230 9.318 1.00 21.92                          ATOM 364 CG ASN A 50 0 6.198 50.569 9.471 1.00 22.44                          ATOM 365 OD1 ASN A 50 0 5.818 49.801 8.572 1.00 24.19                         ATOM 366 ND2 ASN A 50 0 5.435 50.833 10.526 1.00 20.19                        ATOM 367 N ASP A 51 0 7.915 49.959 5.926 1.00 26.42                           ATOM 368 CA ASP A 51 0 7.208 50.071 4.641 1.00 26.35                          ATOM 369 C ASP A 51 0 5.951 49.200 4.600 1.00 24.86                           ATOM 370 O ASP A 51 0 5.542 48.810 3.511 1.00 25.19                           ATOM 371 CB ASP A 51 0 8.126 49.698 3.481 1.00 26.75                          ATOM 372 CG ASP A 51 0 9.152 50.761 3.158 1.00 29.77                          ATOM 373 OD1 ASP A 51 0 8.944 51.904 3.617 1.00 31.03                         ATOM 374 OD2 ASP A 51 0 10.166 50.509 2.465 1.00 30.42                        ATOM 375 N LEU A 52 0 5.332 48.801 5.700 1.00 25.05                           ATOM 376 CA LEU A 52 0 4.172 47.911 5.640 1.00 25.44                          ATOM 377 C LEU A 52 0 2.934 48.624 5.094 1.00 26.65                           ATOM 378 O LEU A 52 0 2.553 49.696 5.586 1.00 24.56                           ATOM 379 CB LEU A 52 0 3.837 47.374 7.029 1.00 24.19                          ATOM 380 CG LEU A 52 0 4.896 46.503 7.699 1.00 24.60                          ATOM 381 CD1 LEU A 52 0 4.611 46.424 9.196 1.00 24.05                         ATOM 382 CD2 LEU A 52 0 4.891 45.119 7.061 1.00 23.49                         ATOM 383 N ASP A 53 0 2.242 47.980 4.169 1.00 28.79                           ATOM 384 CA ASP A 53 0 1.049 48.602 3.581 1.00 29.91                          ATOM 385 C ASP A 53 0 -0.135 47.658 3.492 1.00 29.90                          ATOM 386 O ASP A 53 0 -1.152 48.082 2.951 1.00 30.40                          ATOM 387 CB ASP A 53 0 1.367 49.190 2.197 1.00 29.26                          ATOM 388 CG ASP A 53 0 1.838 48.140 1.218 1.00 31.28                          ATOM 389 OD1 ASP A 53 0 1.865 46.926 1.540 1.00 31.64                         ATOM 390 OD2 ASP A 53 0 2.233 48.474 0.074 1.00 32.42                         ATOM 391 N ASN A 54 0 -0.060 46.437 4.014 1.00 29.44                          ATOM 392 CA ASN A 54 0 -1.237 45.554 3.983 1.00 26.89                         ATOM 393 C ASN A 54 0 -2.089 45.832 5.192 1.00 27.37                          ATOM 394 O ASN A 54 0 -1.772 45.528 6.350 1.00 27.99                          ATOM 395 CB ASN A 54 0 -0.831 44.095 3.913 1.00 25.11                         ATOM 396 CG ASN A 54 0 -1.978 43.141 3.690 1.00 24.20                         ATOM 397 OD1 ASN A 54 0 -1.874 42.344 2.746 1.00 25.13                        ATOM 398 ND2 ASN A 54 0 -3.030 43.182 4.481 1.00 23.26                        ATOM 399 N PRO A 55 0 -3.337 46.256 4.961 1.00 28.44                          ATOM 400 CA PRO A 55 0 -4.286 46.589 6.014 1.00 26.57                         ATOM 401 C PRO A 55 0 -4.909 45.414 6.723 1.00 27.10                          ATOM 402 O PRO A 55 0 -5.671 45.624 7.687 1.00 26.05                          ATOM 403 CB PRO A 55 0 -5.368 47.465 5.334 1.00 28.18                         ATOM 404 CG PRO A 55 0 -5.249 47.049 3.899 1.00 27.50                         ATOM 405 CD PRO A 55 0 -3.844 46.564 3.625 1.00 27.56                         ATOM 406 N THR A 56 0 -4.603 44.160 6.345 1.00 25.55                          ATOM 407 CA THR A 56 0 -5.214 43.024 7.065 1.00 25.52                         ATOM 408 C THR A 56 0 -4.446 42.647 8.326 1.00 24.87                          ATOM 409 O THR A 56 0 -4.766 41.764 9.115 1.00 23.97                          ATOM 410 CB THR A 56 0 -5.393 41.807 6.154 1.00 25.10                         ATOM 411 OG1 THR A 56 0 -4.100 41.345 5.763 1.00 24.26                        ATOM 412 CG2 THR A 56 0 -6.178 42.123 4.861 1.00 25.63                        ATOM 413 N MET A 57 0 -3.317 43.311 8.558 1.00 26.01                          ATOM 414 CA MET A 57 0 -2.553 43.099 9.801 1.00 26.57                         ATOM 415 C MET A 57 0 -2.026 44.475 10.201 1.00 25.88                         ATOM 416 O MET A 57 0 -2.026 45.416 9.397 1.00 25.18                          ATOM 417 CB MET A 57 0 -1.561 41.939 9.698 1.00 25.42                         ATOM 418 CG MET A 57 0 -0.639 41.868 8.554 1.00 24.37                         ATOM 419 SD MET A 57 0 -0.034 40.288 7.916 1.00 22.34                         ATOM 420 CE MET A 57 0 -0.275 40.640 6.167 1.00 19.23                         ATOM 421 N LEU A 58 0 -1.694 44.601 11.476 1.00 25.98                         ATOM 422 CA LEU A 58 0 -1.180 45.850 12.036 1.00 25.57                        ATOM 423 C LEU A 58 0 -0.053 46.425 11.195 1.00 24.52                         ATOM 424 O LEU A 58 0 0.824 45.739 10.638 1.00 23.63                          ATOM 425 CB LEU A 58 0 -0.757 45.535 13.463 1.00 26.67                        ATOM 426 CG LEU A 58 0 -1.628 45.817 14.657 1.00 28.97                        ATOM 427 CD1 LEU A 58 0 -3.107 45.995 14.312 1.00 30.99                       ATOM 428 CD2 LEU A 58 0 -1.488 44.756 15.736 1.00 28.36                       ATOM 429 N ARG A 59 0 -0.078 47.741 11.030 1.00 24.96                         ATOM 430 CA ARG A 59 0 0.918 48.434 10.231 1.00 26.92                         ATOM 431 C ARG A 59 0 1.932 49.229 11.014 1.00 26.31                          ATOM 432 O ARG A 59 0 3.120 49.198 10.699 1.00 28.82                          ATOM 433 CB ARG A 59 0 0.260 49.277 9.132 1.00 28.35                          ATOM 434 CG ARG A 59 0 -0.252 48.385 7.986 1.00 29.50                         ATOM 435 CD ARG A 59 0 -0.986 49.274 6.996 1.00 30.33                         ATOM 436 NE ARG A 59 0 -2.333 49.604 7.459 1.00 32.26                         ATOM 437 CZ ARG A 59 0 -3.121 50.525 6.883 1.00 33.24                         ATOM 438 NH1 ARG A 59 0 -2.679 51.233 5.845 1.00 32.27                        ATOM 439 NH2 ARG A 59 0 -4.340 50.712 7.389 1.00 32.65                        ATOM 440 N PRO A 60 0 1.542 49.961 12.020 1.00 26.30                          ATOM 441 CA PRO A 60 0 2.460 50.669 12.916 1.00 26.19                         ATOM 442 C PRO A 60 0 3.312 49.591 13.595 1.00 25.29                          ATOM 443 O PRO A 60 0 2.879 48.432 13.668 1.00 24.63                          ATOM 444 CB PRO A 60 0 1.623 51.464 13.925 1.00 25.93                         ATOM 445 CG PRO A 60 0 0.235 51.357 13.325 1.00 26.19                         ATOM 446 CD PRO A 60 0 0.165 50.073 12.508 1.00 26.23                         ATOM 447 N THR A 61 0 4.544 49.932 13.976 1.00 24.60                          ATOM 448 CA THR A 61 0 5.365 48.871 14.587 1.00 23.49                         ATOM 449 C THR A 61 0 6.204 49.400 15.743 1.00 22.83                          ATOM 450 O THR A 61 0 6.390 50.601 15.921 1.00 20.77                          ATOM 451 CB THR A 61 0 6.245 48.170 13.535 1.00 22.69                         ATOM 452 OG1 THR A 61 0 6.668 46.918 14.096 1.00 23.55                        ATOM 453 CG2 THR A 61 0 7.444 48.976 13.119 1.00 20.92                        ATOM 454 N SER A 62 0 6.702 48.449 16.507 1.00 22.38                          ATOM 455 CA SER A 62 0 7.599 48.672 17.633 1.00 22.47                         ATOM 456 C SER A 62 0 8.381 47.380 17.893 1.00 22.12                          ATOM 457 O SER A 62 0 7.763 46.331 18.124 1.00 20.53                          ATOM 458 CB SER A 62 0 6.784 49.033 18.882 1.00 22.02                         ATOM 459 OG SER A 62 0 7.666 49.570 19.832 1.00 21.19                         ATOM 460 N ILE A 63 0 9.716 47.451 17.806 1.00 21.17                          ATOM 461 CA ILE A 63 0 10.513 46.240 17.960 1.00 18.32                        ATOM 462 C ILE A 63 0 11.095 46.034 19.354 1.00 18.28                         ATOM 463 O ILE A 63 0 11.832 46.909 19.826 1.00 19.63                         ATOM 464 CB ILE A 63 0 11.642 46.234 16.924 1.00 16.68                        ATOM 465 CG1 ILE A 63 0 11.166 46.509 15.508 1.00 18.51                       ATOM 466 CG2 ILE A 63 0 12.319 44.848 16.906 1.00 16.78                       ATOM 467 CD1 ILE A 63 0 10.055 45.625 14.994 1.00 18.25                       ATOM 468 N HIS A 64 0 10.880 44.890 19.985 1.00 15.18                         ATOM 469 CA HIS A 64 0 11.478 44.539 21.261 1.00 15.51                        ATOM 470 C HIS A 64 0 12.648 43.559 21.029 1.00 16.73                         ATOM 471 O HIS A 64 0 12.491 42.591 20.279 1.00 16.85                         ATOM 472 CB HIS A 64 0 10.512 43.912 22.239 1.00 14.37                        ATOM 473 CG HIS A 64 0 11.033 43.420 23.546 1.00 14.47                        ATOM 474 ND1 HIS A 64 0 11.763 44.191 24.410 1.00 12.89                       ATOM 475 CD2 HIS A 64 0 10.883 42.223 24.193 1.00 14.85                       ATOM 476 CE1 HIS A 64 0 12.067 43.518 25.498 1.00 11.53                       ATOM 477 NE2 HIS A 64 0 11.547 42.325 25.423 1.00 13.63                       ATOM 478 N TRP A 65 0 13.761 43.781 21.723 1.00 14.37                         ATOM 479 CA TRP A 65 0 14.966 42.926 21.577 1.00 13.92                        ATOM 480 C TRP A 65 0 14.987 42.084 22.840 1.00 13.50                         ATOM 481 O TRP A 65 0 15.482 42.538 23.901 1.00 12.84                         ATOM 482 CB TRP A 65 0 16.189 43.825 21.371 1.00 13.50                        ATOM 483 CG TRP A 65 0 15.890 45.020 20.492 1.00 13.19                        ATOM 484 CD1 TRP A 65 0 15.453 46.247 20.913 1.00 12.42                       ATOM 485 CD2 TRP A 65 0 15.908 45.087 19.068 1.00 13.61                       ATOM 486 NE1 TRP A 65 0 15.234 47.067 19.862 1.00 11.49                       ATOM 487 CE2 TRP A 65 0 15.511 46.390 18.710 1.00 13.77                       ATOM 488 CE3 TRP A 65 0 16.251 44.174 18.061 1.00 14.35                       ATOM 489 CZ2 TRP A 65 0 15.439 46.815 17.378 1.00 14.99                       ATOM 490 CZ3 TRP A 65 0 16.169 44.572 16.735 1.00 13.99                       ATOM 491 CH2 TRP A 65 0 15.756 45.869 16.411 1.00 15.82                       ATOM 492 N HIS A 66 0 14.295 40.941 22.747 1.00 10.39                         ATOM 493 CA HIS A 66 0 13.939 40.200 23.966 1.00 12.00                        ATOM 494 C HIS A 66 0 15.158 39.653 24.698 1.00 11.34                         ATOM 495 O HIS A 66 0 15.889 38.859 24.130 1.00 11.51                         ATOM 496 CB HIS A 66 0 12.923 39.069 23.629 1.00 10.76                        ATOM 497 CG HIS A 66 0 12.418 38.308 24.808 1.00 11.26                        ATOM 498 ND1 HIS A 66 0 11.106 38.085 25.092 1.00 13.10                       ATOM 499 CD2 HIS A 66 0 13.050 37.676 25.824 1.00 13.49                       ATOM 500 CE1 HIS A 66 0 10.919 37.407 26.191 1.00 12.50                       ATOM 501 NE2 HIS A 66 0 12.116 37.146 26.683 1.00 13.71                       ATOM 502 N GLY A 67 0 15.345 39.971 25.948 1.00 12.84                         ATOM 503 CA GLY A 67 0 16.492 39.469 26.719 1.00 13.36                        ATOM 504 C GLY A 67 0 17.596 40.500 26.914 1.00 13.11                         ATOM 505 O GLY A 67 0 18.435 40.289 27.788 1.00 13.36                         ATOM 506 N LEU A 68 0 17.641 41.558 26.131 1.00 12.89                         ATOM 507 CA LEU A 68 0 18.659 42.598 26.300 1.00 15.22                        ATOM 508 C LEU A 68 0 18.235 43.501 27.448 1.00 16.14                         ATOM 509 O LEU A 68 0 17.029 43.842 27.505 1.00 16.50                         ATOM 510 CB LEU A 68 0 18.929 43.320 24.988 1.00 15.98                        ATOM 511 CG LEU A 68 0 20.002 42.638 24.114 1.00 19.57                        ATOM 512 CD1 LEU A 68 0 19.719 41.185 23.809 1.00 20.39                       ATOM 513 CD2 LEU A 68 0 20.188 43.316 22.758 1.00 19.59                       ATOM 514 N PHE A 69 0 19.125 43.848 28.386 1.00 13.24                         ATOM 515 CA PHE A 69 0 18.700 44.657 29.526 1.00 13.85                        ATOM 516 C PHE A 69 0 18.499 46.128 29.205 1.00 14.34                         ATOM 517 O PHE A 69 0 17.806 46.879 29.895 1.00 15.02                         ATOM 518 CB PHE A 69 0 19.770 44.579 30.637 1.00 16.02                        ATOM 519 CG PHE A 69 0 20.112 43.187 31.072 1.00 16.45                        ATOM 520 CD1 PHE A 69 0 19.172 42.162 31.026 1.00 16.68                       ATOM 521 CD2 PHE A 69 0 21.381 42.927 31.578 1.00 16.78                       ATOM 522 CE1 PHE A 69 0 19.504 40.883 31.448 1.00 18.86                       ATOM 523 CE2 PHE A 69 0 21.717 41.652 32.001 1.00 17.34                       ATOM 524 CZ PHE A 69 0 20.782 40.628 31.932 1.00 18.09                        ATOM 525 N GLN A 70 0 19.081 46.611 28.130 1.00 12.22                         ATOM 526 CA GLN A 70 0 18.919 47.990 27.708 1.00 15.20                        ATOM 527 C GLN A 70 0 19.242 49.004 28.799 1.00 16.76                         ATOM 528 O GLN A 70 0 18.555 50.016 28.919 1.00 16.08                         ATOM 529 CB GLN A 70 0 17.488 48.115 27.232 1.00 15.52                        ATOM 530 CG GLN A 70 0 17.168 47.303 26.003 1.00 17.37                        ATOM 531 CD GLN A 70 0 17.781 47.744 24.709 1.00 17.70                        ATOM 532 OE1 GLN A 70 0 17.557 47.090 23.676 1.00 21.63                       ATOM 533 NE2 GLN A 70 0 18.549 48.805 24.620 1.00 16.79                       ATOM 534 N ARG A 71 0 20.338 48.804 29.518 1.00 16.49                         ATOM 535 CA ARG A 71 0 20.765 49.712 30.588 1.00 18.41                        ATOM 536 C ARG A 71 0 21.239 51.011 29.970 1.00 16.23                         ATOM 537 O ARG A 71 0 22.059 50.998 29.027 1.00 14.48                         ATOM 538 CB ARG A 71 0 21.827 48.942 31.382 1.00 22.65                        ATOM 539 CG ARG A 71 0 22.273 49.589 32.671 1.00 29.50                        ATOM 540 CD ARG A 71 0 23.286 48.756 33.457 1.00 32.92                        ATOM 541 NE ARG A 71 0 22.712 47.550 34.035 1.00 38.11                        ATOM 542 CZ ARG A 71 0 22.551 46.358 33.452 1.00 40.14                        ATOM 543 NH1 ARG A 71 0 22.939 46.138 32.190 1.00 41.23                       ATOM 544 NH2 ARG A 71 0 22.022 45.333 34.130 1.00 40.89                       ATOM 545 N GLY A 72 0 20.613 52.145 30.311 1.00 14.82                         ATOM 546 CA GLY A 72 0 20.981 53.414 29.676 1.00 14.51                        ATOM 547 C GLY A 72 0 20.268 53.606 28.338 1.00 15.55                         ATOM 548 O GLY A 72 0 20.401 54.706 27.777 1.00 16.32                         ATOM 549 N THR A 73 0 19.503 52.651 27.804 1.00 12.12                         ATOM 550 CA THR A 73 0 18.857 52.781 26.516 1.00 12.50                        ATOM 551 C THR A 73 0 17.418 52.252 26.621 1.00 13.98                         ATOM 552 O THR A 73 0 16.890 51.534 25.776 1.00 13.81                         ATOM 553 CB THR A 73 0 19.577 52.086 25.346 1.00 12.21                        ATOM 554 OG1 THR A 73 0 19.854 50.711 25.666 1.00 12.83                       ATOM 555 CG2 THR A 73 0 20.944 52.711 25.000 1.00 9.81                        ATOM 556 N ASN A 74 0 16.744 52.617 27.708 1.00 12.97                         ATOM 557 CA ASN A 74 0 15.354 52.273 27.951 1.00 14.93                        ATOM 558 C ASN A 74 0 14.469 52.718 26.784 1.00 15.92                         ATOM 559 O ASN A 74 0 13.501 52.030 26.455 1.00 16.56                         ATOM 560 CB ASN A 74 0 14.851 52.821 29.271 1.00 13.06                        ATOM 561 CG ASN A 74 0 13.385 52.519 29.556 1.00 15.47                        ATOM 562 OD1 ASN A 74 0 12.557 53.250 29.021 1.00 13.99                       ATOM 563 ND2 ASN A 74 0 13.063 51.500 30.367 1.00 13.91                       ATOM 564 N TRP A 75 0 14.806 53.765 26.041 1.00 16.16                         ATOM 565 CA TRP A 75 0 14.036 54.262 24.917 1.00 16.49                        ATOM 566 C TRP A 75 0 14.050 53.345 23.701 1.00 17.29                         ATOM 567 O TRP A 75 0 13.235 53.529 22.776 1.00 16.34                         ATOM 568 CB TRP A 75 0 14.516 55.657 24.509 1.00 15.90                        ATOM 569 CG TRP A 75 0 15.990 55.705 24.207 1.00 16.04                        ATOM 570 CD1 TRP A 75 0 17.011 55.972 25.072 1.00 14.90                       ATOM 571 CD2 TRP A 75 0 16.584 55.475 22.916 1.00 15.94                       ATOM 572 NE1 TRP A 75 0 18.210 55.917 24.384 1.00 15.89                       ATOM 573 CE2 TRP A 75 0 17.977 55.624 23.076 1.00 15.80                       ATOM 574 CE3 TRP A 75 0 16.060 55.171 21.656 1.00 14.88                       ATOM 575 CZ2 TRP A 75 0 18.867 55.459 22.016 1.00 17.60                       ATOM 576 CZ3 TRP A 75 0 16.928 55.025 20.603 1.00 16.64                       ATOM 577 CH2 TRP A 75 0 18.321 55.153 20.785 1.00 18.16                       ATOM 578 N ALA A 76 0 14.962 52.372 23.675 1.00 15.12                         ATOM 579 CA ALA A 76 0 15.075 51.430 22.578 1.00 14.61                        ATOM 580 C ALA A 76 0 14.569 50.047 22.971 1.00 13.98                         ATOM 581 O ALA A 76 0 14.617 49.132 22.159 1.00 14.20                         ATOM 582 CB ALA A 76 0 16.554 51.354 22.157 1.00 13.68                        ATOM 583 N ASP A 77 0 13.941 49.885 24.121 1.00 14.47                         ATOM 584 CA ASP A 77 0 13.409 48.605 24.586 1.00 14.23                        ATOM 585 C ASP A 77 0 12.198 48.167 23.762 1.00 15.04                         ATOM 586 O ASP A 77 0 11.982 46.946 23.638 1.00 13.78                         ATOM 587 CB ASP A 77 0 13.112 48.567 26.072 1.00 13.41                        ATOM 588 CG ASP A 77 0 12.945 47.155 26.612 1.00 14.93                        ATOM 589 OD1 ASP A 77 0 11.943 46.986 27.345 1.00 15.07                       ATOM 590 OD2 ASP A 77 0 13.744 46.217 26.334 1.00 13.73                       ATOM 591 N GLY A 78 0 11.458 49.095 23.160 1.00 13.63                         ATOM 592 CA GLY A 78 0 10.442 48.686 22.210 1.00 14.96                        ATOM 593 C GLY A 78 0 9.040 48.309 22.631 1.00 16.75                          ATOM 594 O GLY A 78 0 8.276 47.865 21.755 1.00 16.49                          ATOM 595 N ALA A 79 0 8.631 48.436 23.886 1.00 15.34                          ATOM 596 CA ALA A 79 0 7.252 48.176 24.270 1.00 14.70                         ATOM 597 C ALA A 79 0 6.490 49.495 24.084 1.00 17.51                          ATOM 598 O ALA A 79 0 6.690 50.486 24.807 1.00 17.05                          ATOM 599 CB ALA A 79 0 7.145 47.701 25.708 1.00 14.78                         ATOM 600 N ASP A 80 0 5.641 49.536 23.053 1.00 18.56                          ATOM 601 CA ASP A 80 0 4.859 50.741 22.798 1.00 19.52                         ATOM 602 C ASP A 80 0 3.959 50.963 24.010 1.00 17.61                          ATOM 603 O ASP A 80 0 3.530 49.999 24.664 1.00 16.72                          ATOM 604 CB ASP A 80 0 4.044 50.714 21.510 1.00 24.02                         ATOM 605 CG ASP A 80 0 3.003 49.607 21.549 1.00 28.13                         ATOM 606 OD1 ASP A 80 0 3.410 48.417 21.541 1.00 30.66                        ATOM 607 OD2 ASP A 80 0 1.803 49.959 21.603 1.00 30.61                        ATOM 608 N GLY A 81 0 3.776 52.242 24.337 1.00 15.85                          ATOM 609 CA GLY A 81 0 2.991 52.566 25.532 1.00 16.27                         ATOM 610 C GLY A 81 0 3.846 52.615 26.784 1.00 18.72                          ATOM 611 O GLY A 81 0 3.405 52.983 27.890 1.00 20.61                          ATOM 612 N VAL A 82 0 5.108 52.173 26.725 1.00 19.11                          ATOM 613 CA VAL A 82 0 5.978 52.119 27.890 1.00 19.14                         ATOM 614 C VAL A 82 0 7.288 52.851 27.590 1.00 18.41                          ATOM 615 O VAL A 82 0 7.594 53.839 28.242 1.00 16.79                          ATOM 616 CB VAL A 82 0 6.266 50.697 28.390 1.00 19.82                         ATOM 617 CG1 VAL A 82 0 7.059 50.741 29.710 1.00 21.37                        ATOM 618 CG2 VAL A 82 0 4.995 49.894 28.640 1.00 19.27                        ATOM 619 N ASN A 83 0 7.982 52.408 26.551 1.00 17.90                          ATOM 620 CA ASN A 83 0 9.271 52.926 26.147 1.00 16.94                         ATOM 621 C ASN A 83 0 9.226 53.778 24.886 1.00 18.32                          ATOM 622 O ASN A 83 0 10.175 54.551 24.634 1.00 20.58                         ATOM 623 CB ASN A 83 0 10.249 51.747 25.937 1.00 15.23                        ATOM 624 CG ASN A 83 0 10.112 50.745 27.063 1.00 16.00                        ATOM 625 OD1 ASN A 83 0 9.493 49.676 26.879 1.00 14.98                        ATOM 626 ND2 ASN A 83 0 10.583 51.131 28.249 1.00 13.17                       ATOM 627 N GLN A 84 0 8.183 53.668 24.066 1.00 16.40                          ATOM 628 CA GLN A 84 0 8.080 54.464 22.867 1.00 16.34                         ATOM 629 C GLN A 84 0 6.658 54.465 22.309 1.00 17.95                          ATOM 630 O GLN A 84 0 5.816 53.679 22.728 1.00 17.69                          ATOM 631 CB GLN A 84 0 8.995 53.953 21.754 1.00 17.98                         ATOM 632 CG GLN A 84 0 8.456 52.654 21.127 1.00 16.63                         ATOM 633 CD GLN A 84 0 9.272 52.225 19.938 1.00 18.17                         ATOM 634 OE1 GLN A 84 0 8.994 52.601 18.792 1.00 20.91                        ATOM 635 NE2 GLN A 84 0 10.279 51.385 20.096 1.00 18.70                       ATOM 636 N CYS A 85 0 6.419 55.350 21.365 1.00 18.60                          ATOM 637 CA CYS A 85 0 5.140 55.344 20.622 1.00 20.25                         ATOM 638 C CYS A 85 0 5.512 54.555 19.375 1.00 19.55                          ATOM 639 O CYS A 85 0 6.690 54.546 18.995 1.00 18.92                          ATOM 640 CB CYS A 85 0 4.772 56.786 20.228 1.00 22.20                         ATOM 641 SG CYS A 85 0 3.899 57.783 21.481 1.00 24.65                         ATOM 642 N PRO A 86 0 4.589 53.951 18.674 1.00 21.19                          ATOM 643 CA PRO A 86 0 4.869 53.152 17.498 1.00 20.78                         ATOM 644 C PRO A 86 0 5.560 53.930 16.394 1.00 21.46                          ATOM 645 O PRO A 86 0 5.453 55.137 16.298 1.00 23.08                          ATOM 646 CB PRO A 86 0 3.530 52.555 17.028 1.00 19.94                         ATOM 647 CG PRO A 86 0 2.667 52.720 18.252 1.00 19.59                         ATOM 648 CD PRO A 86 0 3.174 53.872 19.062 1.00 20.46                         ATOM 649 N ILE A 87 0 6.318 53.259 15.550 1.00 20.95                          ATOM 650 CA ILE A 87 0 6.907 53.773 14.337 1.00 22.43                         ATOM 651 C ILE A 87 0 5.768 53.641 13.292 1.00 22.80                          ATOM 652 O ILE A 87 0 5.148 52.562 13.228 1.00 21.61                          ATOM 653 CB ILE A 87 0 8..105 52.954 13.844 1.00 21.99                        ATOM 654 CG1 ILE A 87 0 9.130 52.696 14.944 1.00 24.18                        ATOM 655 CG2 ILE A 87 0 8.773 53.656 12.674 1.00 22.91                        ATOM 656 CD1 ILE A 87 0 10.256 51.776 14.514 1.00 23.87                       ATOM 657 N SER A 88 0 5.464 54.702 12.570 1.00 22.64                          ATOM 658 CA SER A 88 0 4.338 54.709 11.647 1.00 22.85                         ATOM 659 C SER A 88 0 4.751 54.268 10.249 1.00 23.35                          ATOM 660 O SER A 88 0 5.870 54.489 9.764 1.00 23.30                           ATOM 661 CB SER A 88 0 3.767 56.137 11.518 1.00 24.00                         ATOM 662 OG SER A 88 0 3.379 56.770 12.720 1.00 23.93                         ATOM 663 N PRO A 89 0 3.778 53.752 9.514 1.00 23.60                           ATOM 664 CA PRO A 89 0 3.955 53.382 8.116 1.00 25.19                          ATOM 665 C PRO A 89 0 4.579 54.556 7.361 1.00 26.58                           ATOM 666 O PRO A 89 0 4.177 55.699 7.585 1.00 26.66                           ATOM 667 CB PRO A 89 0 2.566 53.065 7.555 1.00 23.59                          ATOM 668 CG PRO A 89 0 1.740 52.856 8.798 1.00 22.37                          ATOM 669 CD PRO A 89 0 2.415 53.513 9.970 1.00 23.25                          ATOM 670 N GLY A 90 0 5.588 54.311 6.550 1.00 27.73                           ATOM 671 CA GLY A 90 0 6.223 55.338 5.748 1.00 30.55                          ATOM 672 C GLY A 90 0 7.384 56.032 6.438 1.00 32.38                           ATOM 673 O GLY A 90 0 8.050 56.894 5.879 1.00 32.53                           ATOM 674 N HIS A 91 0 7.639 55.693 7.702 1.00 32.77                           ATOM 675 CA HIS A 91 0 8.691 56.283 8.494 1.00 32.55                          ATOM 676 C HIS A 91 0 9.649 55.179 8.982 1.00 32.36                           ATOM 677 O HIS A 91 0 9.381 53.972 8.961 1.00 31.30                           ATOM 678 CB HIS A 91 0 8.118 57.016 9.722 1.00 33.75                          ATOM 679 CG HIS A 91 0 7.147 58.073 9.295 1.00 34.64                          ATOM 680 ND1 HIS A 91 0 7.519 59.381 9.072 1.00 34.41                         ATOM 681 CD2 HIS A 91 0 5.822 57.977 9.002 1.00 34.89                         ATOM 682 CE1 HIS A 91 0 6.450 60.050 8.679 1.00 34.87                         ATOM 683 NE2 HIS A 91 0 5.410 59.233 8.628 1.00 35.14                         ATOM 684 N ALA A 92 0 10.786 55.668 9.437 1.00 29.57                          ATOM 685 CA ALA A 92 0 11.895 54.898 9.937 1.00 27.71                         ATOM 686 C ALA A 92 0 12.316 55.347 11.337 1.00 27.41                         ATOM 687 O ALA A 92 0 12.076 56.484 11.741 1.00 26.12                         ATOM 688 CB ALA A 92 0 13.051 55.057 8.967 1.00 25.23                         ATOM 689 N PHE A 93 0 12.931 54.418 12.081 1.00 26.87                         ATOM 690 CA PHE A 93 0 13.441 54.760 13.405 1.00 25.87                        ATOM 691 C PHE A 93 0 14.746 54.008 13.632 1.00 25.21                         ATOM 692 O PHE A 93 0 14.797 52.810 13.347 1.00 25.80                         ATOM 693 CB PHE A 93 0 12.457 54.456 14.526 1.00 25.30                        ATOM 694 CG PHE A 93 0 12.964 54.955 15.847 1.00 25.41                        ATOM 695 CD1 PHE A 93 0 13.154 56.309 16.061 1.00 25.36                       ATOM 696 CD2 PHE A 93 0 13.276 54.057 16.853 1.00 25.31                       ATOM 697 CE1 PHE A 93 0 13.637 56.753 17.285 1.00 26.54                       ATOM 698 CE2 PHE A 93 0 13.754 54.503 18.078 1.00 25.39                       ATOM 699 CZ PHE A 93 0 13.935 55.857 18.302 1.00 25.01                        ATOM 700 N LEU A 94 0 15.756 54.699 14.136 1.00 23.39                         ATOM 701 CA LEU A 94 0 17.046 54.058 14.361 1.00 23.35                        ATOM 702 C LEU A 94 0 17.191 53.611 15.804 1.00 23.22                         ATOM 703 O LEU A 94 0 17.261 54.431 16.714 1.00 23.47                         ATOM 704 CB LEU A 94 0 18.186 54.994 13.943 1.00 24.96                        ATOM 705 CG LEU A 94 0 19.630 54.555 14.170 1.00 26.28                        ATOM 706 CD1 LEU A 94 0 19.979 53.313 13.352 1.00 25.99                       ATOM 707 CD2 LEU A 94 0 20.627 55.678 13.887 1.00 26.06                       ATOM 708 N TYR A 95 0 17.261 52.293 16.023 1.00 21.81                         ATOM 709 CA TYR A 95 0 17.481 51.780 17.379 1.00 19.72                        ATOM 710 C TYR A 95 0 18.991 51.663 17.585 1.00 20.90                         ATOM 711 O TYR A 95 0 19.690 51.248 16.656 1.00 20.74                         ATOM 712 CB TYR A 95 0 16.831 50.448 17.609 1.00 17.86                        ATOM 713 CG TYR A 95 0 15.329 50.411 17.691 1.00 16.35                        ATOM 714 CD1 TYR A 95 0 14.541 50.288 16.535 1.00 16.89                       ATOM 715 CD2 TYR A 95 0 14.701 50.442 18.911 1.00 15.71                       ATOM 716 CE1 TYR A 95 0 13.157 50.205 16.621 1.00 17.21                       ATOM 717 CE2 TYR A 95 0 13.325 50.362 19.033 1.00 16.25                       ATOM 718 CZ TYR A 95 0 12.568 50.266 17.874 1.00 17.97                        ATOM 719 OH TYR A 95 0 11.205 50.189 18.001 1.00 18.61                        ATOM 720 N LYS A 96 0 19.475 52.105 18.752 1.00 20.56                         ATOM 721 CA LYS A 96 0 20.917 52.058 18.975 1.00 21.77                        ATOM 722 C LYS A 96 0 21.139 51.519 20.386 1.00 20.91                         ATOM 723 O LYS A 96 0 20.558 52.122 21.286 1.00 21.98                         ATOM 724 CB LYS A 96 0 21.565 53.427 18.960 1.00 22.89                        ATOM 725 CG LYS A 96 0 21.857 54.046 17.609 1.00 26.39                        ATOM 726 CD LYS A 96 0 22.749 55.251 17.923 1.00 30.80                        ATOM 727 CE LYS A 96 0 22.732 56.348 16.884 1.00 32.90                        ATOM 728 NZ LYS A 96 0 23.767 57.378 17.277 1.00 36.06                        ATOM 729 N PHE A 97 0 21.871 50.437 20.520 1.00 18.14                         ATOM 730 CA PHE A 97 0 22.062 49.863 21.854 1.00 18.19                        ATOM 731 C PHE A 97 0 23.276 48.928 21.805 1.00 16.76                         ATOM 732 O PHE A 97 0 23.870 48.700 20.747 1.00 14.19                         ATOM 733 CB PHE A 97 0 20.816 49.067 22.307 1.00 17.34                        ATOM 734 CG PHE A 97 0 20.379 48.026 21.304 1.00 17.56                        ATOM 735 CD1 PHE A 97 0 20.873 46.732 21.348 1.00 16.27                       ATOM 736 CD2 PHE A 97 0 19.451 48.343 20.326 1.00 18.65                       ATOM 737 CE1 PHE A 97 0 20.476 45.801 20.398 1.00 17.76                       ATOM 738 CE2 PHE A 97 0 19.026 47.408 19.386 1.00 18.64                       ATOM 739 CZ PHE A 97 0 19.546 46.120 19.416 1.00 17.55                        ATOM 740 N THR A 98 0 23.552 48.348 22.971 1.00 17.45                         ATOM 741 CA THR A 98 0 24.644 47.359 22.992 1.00 17.00                        ATOM 742 C THR A 98 0 24.304 46.333 24.042 1.00 16.63                         ATOM 743 O THR A 98 0 23.725 46.631 25.090 1.00 15.86                         ATOM 744 CB THR A 98 0 26.028 47.990 23.256 1.00 17.53                        ATOM 745 OG1 THR A 98 0 27.017 46.924 23.372 1.00 19.01                       ATOM 746 CG2 THR A 98 0 26.088 48.807 24.525 1.00 14.85                       ATOM 747 N PRO A 99 0 24.740 45.097 23.831 1.00 15.98                         ATOM 748 CA PRO A 99 0 24.601 44.019 24.787 1.00 15.11                        ATOM 749 C PRO A 99 0 25.445 44.270 26.020 1.00 15.99                         ATOM 750 O PRO A 99 0 25.260 43.633 27.064 1.00 15.94                         ATOM 751 CB PRO A 99 0 25.025 42.717 24.098 1.00 15.83                        ATOM 752 CG PRO A 99 0 25.042 43.140 22.644 1.00 17.12                        ATOM 753 CD PRO A 99 0 25.362 44.627 22.601 1.00 15.68                        ATOM 754 N ALA A 100 0 26.452 45.149 25.932 1.00 17.29                        ATOM 755 CA ALA A 100 0 27.316 45.501 27.050 1.00 16.88                       ATOM 756 C ALA A 100 0 27.919 44.293 27.754 1.00 16.16                        ATOM 757 O ALA A 100 0 27.779 44.187 28.977 1.00 18.13                        ATOM 758 CB ALA A 100 0 26.498 46.292 28.084 1.00 14.96                       ATOM 759 N GLY A 101 0 28.474 43.360 27.033 1.00 16.41                        ATOM 760 CA GLY A 101 0 29.063 42.172 27.599 1.00 17.49                       ATOM 761 C GLY A 101 0 28.130 40.994 27.769 1.00 16.15                        ATOM 762 O GLY A 101 0 28.593 39.930 28.137 1.00 16.57                        ATOM 763 N HIS A 102 0 26.838 41.120 27.521 1.00 17.58                        ATOM 764 CA HIS A 102 0 25.858 40.058 27.804 1.00 15.77                       ATOM 765 C HIS A 102 0 25.707 39.165 26.600 1.00 15.28                        ATOM 766 O HIS A 102 0 25.087 39.641 25.662 1.00 17.64                        ATOM 767 CB HIS A 102 0 24.498 40.666 28.186 1.00 17.95                       ATOM 768 CG HIS A 102 0 23.432 39.661 28.493 1.00 20.00                       ATOM 769 ND1 HIS A 102 0 22.099 40.005 28.547 1.00 20.59                      ATOM 770 CD2 HIS A 102 0 23.475 38.323 28.772 1.00 20.09                      ATOM 771 CE1 HIS A 102 0 21.398 38.937 28.866 1.00 20.77                      ATOM 772 NE2 HIS A 102 0 22.201 37.896 29.016 1.00 20.56                      ATOM 773 N ALA A 103 0 26.277 37.958 26.584 1.00 13.32                        ATOM 774 CA ALA A 103 0 26.141 37.127 25.415 1.00 13.99                       ATOM 775 C ALA A 103 0 24.974 36.156 25.649 1.00 13.43                        ATOM 776 O ALA A 103 0 24.571 35.905 26.784 1.00 11.81                        ATOM 777 CB ALA A 103 0 27.418 36.329 25.151 1.00 16.36                       ATOM 778 N GLY A 104 0 24.459 35.610 24.554 1.00 12.38                        ATOM 779 CA GLY A 104 0 23.381 34.632 24.778 1.00 12.85                       ATOM 780 C GLY A 104 0 22.480 34.451 23.581 1.00 11.06                        ATOM 781 O GLY A 104 0 22.674 35.057 22.515 1.00 10.91                        ATOM 782 N THR A 105 0 21.442 33.650 23.794 1.00 10.14                        ATOM 783 CA THR A 105 0 20.490 33.394 22.704 1.00 10.04                       ATOM 784 C THR A 105 0 19.238 34.236 22.989 1.00 9.52                         ATOM 785 O THR A 105 0 18.738 34.194 24.125 1.00 7.52                         ATOM 786 CB THR A 105 0 20.114 31.913 22.665 1.00 12.67                       ATOM 787 OG1 THR A 105 0 21.273 31.075 22.593 1.00 13.47                      ATOM 788 CG2 THR A 105 0 19.187 31.684 21.468 1.00 12.75                      ATOM 789 N PHE A 106 0 18.842 35.065 22.044 1.00 7.76                         ATOM 790 CA PHE A 106 0 17.731 35.992 22.243 1.00 10.15                       ATOM 791 C PHE A 106 0 16.756 35.910 21.068 1.00 8.42                         ATOM 792 O PHE A 106 0 16.941 35.083 20.166 1.00 8.33                         ATOM 793 CB PHE A 106 0 18.283 37.460 22.369 1.00 10.19                       ATOM 794 CG PHE A 106 0 19.291 37.577 23.506 1.00 12.95                       ATOM 795 CD1 PHE A 106 0 18.905 37.443 24.815 1.00 11.44                      ATOM 796 CD2 PHE A 106 0 20.654 37.775 23.230 1.00 12.37                      ATOM 797 CE1 PHE A 106 0 19.855 37.531 25.822 1.00 14.20                      ATOM 798 CE2 PHE A 106 0 21.574 37.857 24.273 1.00 11.56                      ATOM 799 CZ PHE A 106 0 21.202 37.733 25.599 1.00 9.45                        ATOM 800 N TRP A 107 0 15.869 36.887 20.917 1.00 6.61                         ATOM 801 CA TRP A 107 0 15.062 36.977 19.713 1.00 10.20                       ATOM 802 C TRP A 107 0 14.511 38.398 19.625 1.00 10.63                        ATOM 803 O TRP A 107 0 14.463 39.036 20.657 1.00 13.71                        ATOM 804 CB TRP A 107 0 13.928 35.966 19.636 1.00 7.49                        ATOM 805 CG TRP A 107 0 12.945 35.916 20.755 1.00 9.41                        ATOM 806 CD1 TRP A 107 0 13.136 35.804 22.106 1.00 10.53                      ATOM 807 CD2 TRP A 107 0 11.509 36.004 20.581 1.00 9.17                       ATOM 808 NE1 TRP A 107 0 11.929 35.784 22.768 1.00 10.63                      ATOM 809 CE2 TRP A 107 0 10.924 35.926 21.842 1.00 9.90                       ATOM 810 CE3 TRP A 107 0 10.698 36.144 19.444 1.00 8.77                       ATOM 811 CZ2 TRP A 107 0 9.538 35.947 22.025 1.00 10.01                       ATOM 812 CZ3 TRP A 107 0 9.336 36.167 19.613 1.00 8.60                        ATOM 813 CH2 TRP A 107 0 8.774 36.061 20.890 1.00 10.09                       ATOM 814 N TYR A 108 0 14.117 38.847 18.464 1.00 10.72                        ATOM 815 CA TYR A 108 0 13.498 40.148 18.302 1.00 12.19                       ATOM 816 C TYR A 108 0 12.030 39.869 17.875 1.00 13.62                        ATOM 817 O TYR A 108 0 11.752 38.837 17.245 1.00 13.85                        ATOM 818 CB TYR A 108 0 14.182 40.994 17.259 1.00 11.05                       ATOM 819 CG TYR A 108 0 14.176 40.413 15.857 1.00 13.89                       ATOM 820 CD1 TYR A 108 0 15.087 39.464 15.423 1.00 12.99                      ATOM 821 CD2 TYR A 108 0 13.257 40.897 14.920 1.00 14.94                      ATOM 822 CE1 TYR A 108 0 15.064 38.979 14.130 1.00 13.64                      ATOM 823 CE2 TYR A 108 0 13.216 40.409 13.624 1.00 15.34                      ATOM 824 CZ TYR A 108 0 14.123 39.443 13.236 1.00 14.99                       ATOM 825 OH TYR A 108 0 14.063 38.960 11.946 1.00 16.68                       ATOM 826 N HIS A 109 0 11.123 40.752 18.254 1.00 12.81                        ATOM 827 CA HIS A 109 0 9.735 40.630 17.826 1.00 14.92                        ATOM 828 C HIS A 109 0 9.057 41.988 17.991 1.00 15.96                         ATOM 829 O HIS A 109 0 9.392 42.800 18.875 1.00 15.67                         ATOM 830 CB HIS A 109 0 8.903 39.566 18.550 1.00 12.30                        ATOM 831 CG HIS A 109 0 8.804 39.727 20.036 1.00 12.30                        ATOM 832 ND1 HIS A 109 0 7.788 40.429 20.666 1.00 9.89                        ATOM 833 CD2 HIS A 109 0 9.614 39.264 21.034 1.00 10.76                       ATOM 834 CE1 HIS A 109 0 7.982 40.379 21.971 1.00 8.49                        ATOM 835 NE2 HIS A 109 0 9.086 39.679 22.224 1.00 7.92                        ATOM 836 N SER A 110 0 8.070 42.203 17.122 1.00 16.26                         ATOM 837 CA SER A 110 0 7.244 43.404 17.300 1.00 14.55                        ATOM 838 C SER A 110 0 6.548 43.283 18.646 1.00 13.56                         ATOM 839 O SER A 110 0 6.219 42.191 19.140 1.00 13.54                         ATOM 840 CB SER A 110 0 6.219 43.543 16.159 1.00 16.69                        ATOM 841 OG SER A 110 0 5.212 44.481 16.508 1.00 15.32                        ATOM 842 N HIS A 111 0 6.396 44.395 19.359 1.00 14.60                         ATOM 843 CA HIS A 111 0 5.724 44.397 20.645 1.00 16.23                        ATOM 844 C HIS A 111 0 4.349 45.070 20.478 1.00 18.61                         ATOM 845 O HIS A 111 0 3.713 45.391 21.473 1.00 21.72                         ATOM 846 CB HIS A 111 0 6.478 45.166 21.721 1.00 14.37                        ATOM 847 CG HIS A 111 0 6.392 44.519 23.077 1.00 15.33                        ATOM 848 ND1 HIS A 111 0 5.341 44.660 23.947 1.00 14.55                       ATOM 849 CD2 HIS A 111 0 7.265 43.676 23.680 1.00 14.72                       ATOM 850 CE1 HIS A 111 0 5.589 43.936 25.040 1.00 16.29                       ATOM 851 NE2 HIS A 111 0 6.773 43.326 24.920 1.00 15.35                       ATOM 852 N PHE A 112 0 3.950 45.382 19.258 1.00 18.67                         ATOM 853 CA PHE A 112 0 2.725 46.139 19.037 1.00 19.61                        ATOM 854 C PHE A 112 0 1.540 45.219 18.777 1.00 19.06                         ATOM 855 O PHE A 112 0 1.521 44.630 17.707 1.00 17.50                         ATOM 856 CB PHE A 112 0 2.971 47.113 17.875 1.00 21.16                        ATOM 857 CG PHE A 112 0 1.798 48.019 17.611 1.00 23.12                        ATOM 858 CD1 PHE A 112 0 1.456 49.007 18.509 1.00 24.59                       ATOM 859 CD2 PHE A 112 0 1.034 47.886 16.466 1.00 24.82                       ATOM 860 CE1 PHE A 112 0 G.387 49.852 18.312 1.00 24.29                       ATOM 861 CE2 PHE A 112 0 -0.063 48.714 16.243 1.00 25.87                      ATOM 862 CZ PHE A 112 0 -0.378 49.698 17.161 1.00 25.17                       ATOM 863 N GLY A 113 0 0.599 45.092 19.707 1.00 18.05                         ATOM 864 CA GLY A 113 0 -0.554 44.236 19.433 1.00 19.69                       ATOM 865 C GLY A 113 0 -0.085 42.819 19.096 1.00 22.25                        ATOM 866 O GLY A 113 0 0.937 42.333 19.593 1.00 20.55                         ATOM 867 N THR A 114 0 -0.817 42.173 18.186 1.00 20.91                        ATOM 868 CA THR A 114 0 -0.493 40.816 17.749 1.00 20.85                       ATOM 869 C THR A 114 0 0.296 40.774 16.471 1.00 18.04                         ATOM 870 O THR A 114 0 0.243 39.783 15.743 1.00 18.26                         ATOM 871 CB THR A 114 0 -1.847 40.095 17.487 1.00 23.93                       ATOM 872 OG1 THR A 114 0 -2.609 40.910 16.554 1.00 25.68                      ATOM 873 CG2 THR A 114 0 -2.571 39.926 18.792 1.00 23.72                      ATOM 874 N GLN A 115 0 1.023 41.819 16.095 1.00 17.04                         ATOM 875 CA GLN A 115 0 1.792 41.842 14.853 1.00 16.88                        ATOM 876 C GLN A 115 0 2.881 40.775 14.744 1.00 17.94                         ATOM 877 O GLN A 115 0 3.203 40.263 13.649 1.00 17.18                         ATOM 878 CB GLN A 115 0 2.391 43.244 14.757 1.00 17.55                        ATOM 879 CG GLN A 115 0 3.026 43.601 13.418 1.00 17.65                        ATOM 880 CD GLN A 115 0 3.558 45.024 13.418 1.00 17.73                        ATOM 881 OE1 GLN A 115 0 3.257 45.782 12.482 1.00 19.19                       ATOM 882 NE2 GLN A 115 0 4.334 45.421 14.422 1.00 14.70                       ATOM 883 N TYR A 116 0 3.515 40.416 15.881 1.00 16.32                         ATOM 884 CA TYR A 116 0 4.561 39.386 15.859 1.00 15.92                        ATOM 885 C TYR A 116 0 3.935 38.042 15.479 1.00 17.17                         ATOM 886 O TYR A 116 0 4.584 37.258 14.786 1.00 16.70                         ATOM 887 CB TYR A 116 0 5.411 39.312 17.096 1.00 13.45                        ATOM 888 CG TYR A 116 0 5.209 38.487 18.314 1.00 10.97                        ATOM 889 CD1 TYR A 116 0 5.581 37.146 18.394 1.00 11.02                       ATOM 890 CD2 TYR A 116 0 4.665 39.052 19.460 1.00 12.18                       ATOM 891 CE1 TYR A 116 0 5.364 36.399 19.532 1.00 10.02                       ATOM 892 CE2 TYR A 116 0 4.491 38.345 20.642 1.00 12.25                       ATOM 893 CZ TYR A 116 0 4.838 36.996 20.649 1.00 11.73                        ATOM 894 OH TYR A 116 0 4.642 36.295 21.821 1.00 12.72                        ATOM 895 N CYS A 117 0 2.654 37.829 15.842 1.00 17.70                         ATOM 896 CA CYS A 117 0 1.965 36.617 15.424 1.00 18.01                        ATOM 897 C CYS A 117 0 1.883 36.496 13.911 1.00 17.55                         ATOM 898 O CYS A 117 0 1.796 35.352 13.450 1.00 17.50                         ATOM 899 CB CYS A 117 0 0.565 36.528 16.042 1.00 17.90                        ATOM 900 SG CYS A 117 0 0.463 36.895 17.810 1.00 19.72                        ATOM 901 N ASP A 118 0 2.001 37.568 13.136 1.00 15.51                         ATOM 902 CA ASP A 118 0 1.953 37.509 11.696 1.00 17.74                        ATOM 903 C ASP A 118 0 3.341 37.445 11.061 1.00 18.72                         ATOM 904 O ASP A 118 0 3.494 37.770 9.865 1.00 17.47                          ATOM 905 CB ASP A 118 0 1.142 38.696 11.131 1.00 18.61                        ATOM 906 CG ASP A 118 0 -0.356 38.448 11.378 1.00 21.44                       ATOM 907 OD1 ASP A 118 0 -0.826 37.331 11.082 1.00 21.55                      ATOM 908 OD2 ASP A 118 0 -1.064 39.333 11.885 1.00 21.54                      ATOM 909 N GLY A 119 0 4.355 37.095 11.882 1.00 18.19                         ATOM 910 CA GLY A 119 0 5.671 36.889 11.313 1.00 19.00                        ATOM 911 C GLY A 119 0 6.751 37.898 11.590 1.00 19.79                         ATOM 912 O GLY A 119 0 7.909 37.640 11.213 1.00 19.97                         ATOM 913 N LEU A 120 0 6.445 39.011 12.280 1.00 18.24                         ATOM 914 CA LEU A 120 0 7.484 39.991 12.569 1.00 16.08                        ATOM 915 C LEU A 120 0 8.210 39.565 13.848 1.00 16.53                         ATOM 916 O LEU A 120 0 7.933 40.051 14.939 1.00 15.31                         ATOM 917 CB LEU A 120 0 6.918 41.389 12.654 1.00 16.22                        ATOM 918 CG LEU A 120 0 7.916 42.540 12.830 1.00 17.73                        ATOM 919 CD1 LEU A 120 0 9.188 42.293 12.043 1.00 17.73                       ATOM 920 CD2 LEU A 120 0 7.302 43.880 12.448 1.00 16.66                       ATOM 921 N ARG A 121 0 9.144 38.622 13.682 1.00 14.23                         ATOM 922 CA ARG A 121 0 9.859 37.985 14.773 1.00 14.19                        ATOM 923 C ARG A 121 0 11.007 37.152 14.159 1.00 14.09                        ATOM 924 O ARG A 121 0 10.936 36.787 12.978 1.00 13.72                        ATOM 925 CB ARG A 121 0 8934 37.061 15.581 1.00 12.30                         ATOM 926 CG ARG A 121 0 8.253 35.999 14.728 1.00 12.44                        ATOM 927 CD ARG A 121 0 7.303 35.098 15.518 1.00 11.94                        ATOM 928 NE ARG A 121 0 6.507 34.269 14.604 1.00 12.92                        ATOM 929 CZ ARG A 121 0 5.413 33.570 14.933 1.00 10.55                        ATOM 930 NH1 ARG A 121 0 4.897 33.483 16.137 1.00 8.12                        ATOM 931 NH2 ARG A 121 0 4.803 32.946 13.930 1.00 10.40                       ATOM 932 N GLY A 122 0 12.045 36.848 14.937 1.00 12.29                        ATOM 933 CA GLY A 122 0 13.162 36.078 14.364 1.00 11.42                       ATOM 934 C GLY A 122 0 14.185 35.918 15.486 1.00 12.42                        ATOM 935 O GLY A 122 0 14.095 36.604 16.509 1.00 11.47                        ATOM 936 N PRO A 123 0 15.164 35.075 15.246 1.00 11.82                        ATOM 937 CA PRO A 123 0 16.226 34.778 16.190 1.00 12.81                       ATOM 938 C PRO A 123 0 17.288 35.857 16.258 1.00 12.41                        ATOM 939 O PRO A 123 0 17.565 36.580 15.302 1.00 12.03                        ATOM 940 CB PRO A 123 0 16.833 33.416 15.713 1.00 12.34                       ATOM 941 CG PRO A 123 0 16.567 33.494 14.223 1.00 12.19                       ATOM 942 CD PRO A 123 0 15.283 34.289 14.021 1.00 11.35                       ATOM 943 N MET A 124 0 17.903 36.027 17.431 1.00 14.30                        ATOM 944 CA MET A 124 0 18.959 37.024 17.628 1.00 14.19                       ATOM 945 C MET A 124 0 20.040 36.414 18.528 1.00 15.37                        ATOM 946 O MET A 124 0 19.788 36.067 19.690 1.00 15.41                        ATOM 947 CB MET A 124 0 18.411 38.290 18.242 1.00 15.94                       ATOM 948 CG MET A 124 0 19.464 39.345 18.604 1.00 19.30                       ATOM 949 SD MET A 124 0 18.646 40.875 19.164 1.00 21.94                       ATOM 950 CE MET A 124 0 19.918 42.061 18.729 1.00 23.64                       ATOM 951 N VAL A 125 0 21.212 36.178 17.939 1.00 13.74                        ATOM 952 CA VAL A 125 0 22.282 35.479 18.658 1.00 13.87                       ATOM 953 C VAL A 125 0 23.478 36.390 18.872 1.00 13.68                        ATOM 954 O VAL A 125 0 24.004 36.976 17.945 1.00 14.01                        ATOM 955 CB VAL A 125 0 22.672 34.139 18.005 1.00 12.58                       ATOM 956 CG1 VAL A 125 0 23.787 33.383 18.749 1.00 11.23                      ATOM 957 CG2 VAL A 125 0 21.448 33.212 18.033 1.00 12.14                      ATOM 958 N ILE A 126 0 23.860 36.535 20.135 1.00 14.48                        ATOM 959 CA ILE A 126 0 25.016 37.295 20.557 1.00 14.53                       ATOM 960 C ILE A 126 0 26.131 36.348 21.054 1.00 13.58                        ATOM 961 O ILE A 126 0 26.061 35.791 22.154 1.00 12.93                        ATOM 962 CB ILE A 126 0 24.649 38.295 21.662 1.00 14.95                       ATOM 963 CG1 ILE A 126 0 23.563 39.302 21.254 1.00 15.29                      ATOM 964 CG2 ILE A 126 0 25.901 39.014 22.174 1.00 14.24                      ATOM 965 CD1 ILE A 126 0 23.703 39.905 19.896 1.00 15.84                      ATOM 966 N TYR A 127 0 27.142 36.146 20.236 1.00 13.66                        ATOM 967 CA TYR A 127 0 28.278 35.258 20.529 1.00 14.62                       ATOM 968 C TYR A 127 0 29.328 35.778 21.507 1.00 15.97                        ATOM 969 O TYR A 127 0 29.626 36.977 21.669 1.00 15.27                        ATOM 970 CB TYR A 127 0 28.965 34.939 19.176 1.00 14.97                       ATOM 971 CG TYR A 127 0 28.057 34.136 18.272 1.00 16.10                       ATOM 972 CD1 TYR A 127 0 27.823 32.782 18.496 1.00 14.96                      ATOM 973 CD2 TYR A 127 0 27.428 34.753 17.177 1.00 16.64                      ATOM 974 CE1 TYR A 127 0 26.995 32.057 17.650 1.00 16.16                      ATOM 975 CE2 TYR A 127 0 26.576 34.039 16.356 1.00 17.32                      ATOM 976 CZ TYR A 127 0 26.374 32.692 16.592 1.00 18.16                       ATOM 977 OH TYR A 127 0 25.540 31.971 15.756 1.00 20.32                       ATOM 978 N ASP A 128 0 29.892 34.895 22.312 1.00 14.36                        ATOM 979 CA ASP A 128 0 30.825 35.269 23.365 1.00 16.80                       ATOM 980 C ASP A 128 0 32.222 34.863 22.939 1.00 20.11                        ATOM 981 O ASP A 128 0 32.508 33.656 22.777 1.00 21.41                        ATOM 982 CB ASP A 128 0 30.398 34.568 24.649 1.00 16.65                       ATOM 983 CG ASP A 128 0 31.136 35.055 25.874 1.00 18.36                       ATOM 984 OD1 ASP A 128 0 32.194 35.708 25.750 1.00 18.72                      ATOM 985 OD2 ASP A 128 0 30.710 34.819 27.024 1.00 20.03                      ATOM 986 N ASP A 129 0 33.148 35.798 22.771 1.00 22.30                        ATOM 987 CA ASP A 129 0 34.511 35.389 22.377 1.00 24.39                       ATOM 988 C ASP A 129 0 35.282 34.740 23.509 1.00 22.47                        ATOM 989 O ASP A 129 0 36.275 34.096 23.209 1.00 23.18                        ATOM 990 CB ASP A 129 0 35.298 36.490 21.707 1.00 28.46                       ATOM 991 CG ASP A 129 0 35.372 37.764 22.516 1.00 31.10                       ATOM 992 OD1 ASP A 129 0 35.254 37.652 23.747 1.00 32.87                      ATOM 993 OD2 ASP A 129 0 35.553 38.824 21.891 1.00 34.70                      ATOM 994 N ASN A 130 0 34.829 34.684 24.736 1.00 21.92                        ATOM 995 CA ASN A 130 0 35.368 34.015 25.874 1.00 23.74                       ATOM 996 C ASN A 130 0 34.382 32.976 26.417 1.00 23.02                        ATOM 997 O ASN A 130 0 34.352 32.684 27.616 1.00 20.14                        ATOM 998 CB ASN A 130 0 35.686 35.002 27.028 1.00 26.41                       ATOM 999 CG ASN A 130 0 36.583 36.127 26.550 1.00 30.99                       ATOM 1000 OD1 ASN A 130 0 36.187 37.309 26.486 1.00 33.20                     ATOM 1001 ND2 ASN A 130 0 37.818 35.769 26.175 1.00 30.96                     ATOM 1002 N ASP A 131 0 33.533 32.401 25.561 1.00 23.32                       ATOM 1003 CA ASP A 131 0 32.476 31.543 26.127 1.00 21.63                      ATOM 1004 C ASP A 131 0 33.010 30.514 27.103 1.00 19.56                       ATOM 1005 O ASP A 131 0 33.704 29.569 26.766 1.00 19.71                       ATOM 1006 CB ASP A 131 0 31.594 30.877 25.063 1.00 22.97                      ATOM 1007 CG ASP A 131 0 30.220 30.487 25.591 1.00 24.48                      ATOM 1008 OD1 ASP A 131 0 30.181 29.525 26.397 1.00 26.42                     ATOM 1009 OD2 ASP A 131 0 29.166 31.051 25.212 1.00 22.66                     ATOM 1010 N PRO A 132 0 32.491 30.548 28.315 1.00 18.77                       ATOM 1011 CA PRO A 132 0 32.759 29.611 29.381 1.00 19.41                      ATOM 1012 C PRO A 132 0 32.523 28.141 29.031 1.00 20.89                       ATOM 1013 O PRO A 132 0 33.112 27.250 29.672 1.00 19.99                       ATOM 1014 CB PRO A 132 0 31.799 29.990 30.531 1.00 18.42                      ATOM 1015 CG PRO A 132 0 31.589 31.470 30.263 1.00 16.87                      ATOM 1016 CD PRO A 132 0 31.645 31.673 28.778 1.00 16.73                      ATOM 1017 N HIS A 133 0 31.668 27.836 28.063 1.00 19.47                       ATOM 1018 CA HIS A 133 0 31.331 26.465 27.700 1.00 18.79                      ATOM 1019 C HIS A 133 0 31.887 26.014 26.372 1.00 19.35                       ATOM 1020 O HIS A 133 0 31.503 24.954 25.826 1.00 18.60                       ATOM 1021 CB HIS A 133 0 29.789 26.428 27.536 1.00 18.91                      ATOM 1022 CG HIS A 133 0 29.065 26.242 28.815 1.00 18.13                      ATOM 1023 ND1 HIS A 133 0 29.566 25.551 29.877 1.00 19.52                     ATOM 1024 CD2 HIS A 133 0 27.817 26.625 29.183 1.00 19.38                     ATOM 1025 CE1 HIS A 133 0 28.679 25.530 30.855 1.00 20.08                     ATOM 1026 NE2 HIS A 133 0 27.587 26.180 30.457 1.00 19.60                     ATOM 1027 N ALA A 134 0 32.840 26.801 25.852 1.00 19.40                       ATOM 1028 CA ALA A 134 0 33.413 26.465 24.552 1.00 21.88                      ATOM 1029 C ALA A 134 0 34.080 25.107 24.525 1.00 21.69                       ATOM 1030 O ALA A 134 0 34.120 24.514 23.439 1.00 21.61                       ATOM 1031 CB ALA A 134 0 34.418 27.548 24.128 1.00 22.55                      ATOM 1032 N ALA A 135 0 34.582 24.527 25.622 1.00 21.96                       ATOM 1033 CA ALA A 135 0 35.178 23.192 25.483 1.00 23.53                      ATOM 1034 C ALA A 135 0 34.144 22.096 25.232 1.00 24.47                       ATOM 1035 O ALA A 135 0 34.488 20.936 24.989 1.00 24.77                       ATOM 1036 CB ALA A 135 0 35.910 22.820 26.776 1.00 21.92                      ATOM 1037 N LEU A 136 0 32.862 22.375 25.457 1.00 24.95                       ATOM 1038 CA LEU A 136 0 31.800 21.376 25.404 1.00 23.15                      ATOM 1039 C LEU A 136 0 31.284 21.076 24.016 1.00 20.31                       ATOM 1040 O LEU A 136 0 30.609 20.054 23.924 1.00 19.62                       ATOM 1041 CB LEU A 136 0 30.665 21.845 26.318 1.00 24.43                      ATOM 1042 CG LEU A 136 0 30.501 21.211 27.686 1.00 27.55                      ATOM 1043 CD1 LEU A 136 0 31.803 20.721 28.285 1.00 25.75                     ATOM 1044 CD2 LEU A 136 0 29.747 22.129 28.644 1.00 26.92                     ATOM 1045 N TYR A 137 0 31.565 21.888 22.998 1.00 17.05                       ATOM 1046 CA TYR A 137 0 31.085 21.612 21.662 1.00 16.65                      ATOM 1047 C TYR A 137 0 32.076 22.054 20.599 1.00 17.99                       ATOM 1048 O TYR A 137 0 32.965 22.891 20.794 1.00 18.69                       ATOM 1049 CB TYR A 137 0 29.724 22.319 21.402 1.00 16.73                      ATOM 1050 CG TYR A 137 0 29.711 23.760 21.857 1.00 16.24                      ATOM 1051 CD1 TYR A 137 0 29.302 24.108 23.150 1.00 16.00                     ATOM 1052 CD2 TYR A 137 0 30.159 24.754 21.001 1.00 14.76                     ATOM 1053 CE1 TYR A 137 0 29.355 25.448 23.551 1.00 15.32                     ATOM 1054 CE2 TYR A 137 0 30.165 26.081 21.396 1.00 15.52                     ATOM 1055 CZ TYR A 137 0 29.759 26.410 22.675 1.00 15.61                      ATOM 1056 OH TYR A 137 0 29.782 27.731 23.055 1.00 17.56                      ATOM 1057 N ASP A 138 0 31.903 21.549 19.393 1.00 19.04                       ATOM 1058 CA ASP A 138 0 32.733 21.859 18.253 1.00 20.02                      ATOM 1059 C ASP A 138 0 32.139 22.933 17.364 1.00 21.05                       ATOM 1060 O ASP A 138 0 32.911 23.553 16.631 1.00 21.98                       ATOM 1061 CB ASP A 138 0 32.836 20.628 17.315 1.00 20.66                      ATOM 1062 CG ASP A 138 0 33.355 19.455 18.089 1.00 22.79                      ATOM 1063 OD1 ASP A 138 0 32.744 18.404 18.318 1.00 24.88                     ATOM 1064 OD2 ASP A 138 0 34.481 19.675 18.581 1.00 25.34                     ATOM 1065 N GLU A 139 0 30.825 22.957 17.184 1.00 19.73                       ATOM 1066 CA GLU A 139 0 30.223 23.865 16.213 1.00 21.27                      ATOM 1067 C GLU A 139 0 29.086 24.668 16.825 1.00 18.97                       ATOM 1068 O GLU A 139 0 28.306 24.143 17.608 1.00 16.95                       ATOM 1069 CB GLU A 139 0 29.617 23.164 15.000 1.00 24.71                      ATOM 1070 CG GLU A 139 0 30.509 22.149 14.311 1.00 30.89                      ATOM 1071 CD GLU A 139 0 31.633 22.868 13.587 1.00 34.42                      ATOM 1072 OE1 GLU A 139 0 31.340 23.869 12.898 1.00 36.87                     ATOM 1073 OE2 GLU A 139 0 32.794 22.457 13.705 1.00 37.60                     ATOM 1074 N ASP A 140 0 29.057 25.933 16.408 1.00 19.38                       ATOM 1075 CA ASP A 140 0 28.026 26.847 16.912 1.00 17.89                      ATOM 1076 C ASP A 140 0 27.858 27.901 15.837 1.00 18.87                       ATOM 1077 O ASP A 140 0 28.705 28.780 15.768 1.00 21.31                       ATOM 1078 CB ASP A 140 0 28.438 27.399 18.268 1.00 16.26                      ATOM 1079 CG ASP A 140 0 27.445 28.399 18.858 1.00 16.73                      ATOM 1080 OD1 ASP A 140 0 27.854 29.143 19.781 1.00 14.86                     ATOM 1081 OD2 ASP A 140 0 26.287 28.446 18.401 1.00 13.82                     ATOM 1082 N ASP A 141 0 26.862 27.844 14.972 1.00 17.34                       ATOM 1083 CA ASP A 141 0 26.750 28.859 13.937 1.00 19.52                      ATOM 1084 C ASP A 141 0 25.301 29.031 13.520 1.00 19.33                       ATOM 1085 O ASP A 141 0 24.342 28.513 14.115 1.00 17.91                       ATOM 1086 CB ASP A 141 0 27.681 28.509 12.772 1.00 21.66                      ATOM 1087 CG ASP A 141 0 27.384 27.151 12.193 1.00 24.87                      ATOM 1088 OD1 ASP A 141 0 28.280 26.521 11.567 1.00 28.90                     ATOM 1089 OD2 ASP A 141 0 26.271 26.604 12.302 1.00 25.89                     ATOM 1090 N GLU A 142 0 25.102 29.688 12.387 1.00 19.21                       ATOM 1091 CA GLU A 142 0 23.775 29.945 11.880 1.00 20.84                      ATOM 1092 C GLU A 142 0 23.052 28.636 11.592 1.00 19.95                       ATOM 1093 O GLU A 142 0 21.844 28.656 11.665 1.00 18.73                       ATOM 1094 CB GLU A 142 0 23.771 30.894 10.699 1.00 23.40                      ATOM 1095 CG GLU A 142 0 24.295 30.301 9.407 1.00 27.22                       ATOM 1096 CD GLU A 142 0 25.718 30.826 9.221 1.00 32.36                       ATOM 1097 OE1 GLU A 142 0 26.513 30.920 10.206 1.00 31.87                     ATOM 1098 OE2 GLU A 142 0 25.968 31.136 8.023 1.00 35.76                      ATOM 1099 N ASN A 143 0 23.723 27.508 11.378 1.00 20.40                       ATOM 1100 CA ASN A 143 0 23.105 26.227 11.151 1.00 19.61                      ATOM 1101 C ASN A 143 0 22.785 25.468 12.421 1.00 18.35                       ATOM 1102 O ASN A 143 0 22.317 24.337 12.325 1.00 15.65                       ATOM 1103 CB ASN A 143 0 24.024 25.401 10.229 1.00 23.57                      ATOM 1104 CG ASN A 143 0 24.133 26.067 8.857 1.00 26.63                       ATOM 1105 OD1 ASN A 143 0 25.220 26.376 8.356 1.00 29.89                      ATOM 1106 ND2 ASN A 143 0 23.049 26.342 8.175 1.00 25.46                      ATOM 1107 N THR A 144 0 23.067 25.974 13.632 1.00 16.76                       ATOM 1108 CA THR A 144 0 22.678 25.257 14.825 1.00 15.40                      ATOM 1109 C THR A 144 0 21.556 25.976 15.577 1.00 15.58                       ATOM 1110 O THR A 144 0 21.361 25.776 16.789 1.00 17.88                       ATOM 1111 CB THR A 144 0 23.848 25.018 15.785 1.00 16.43                      ATOM 1112 OG1 THR A 144 0 24.296 26.270 16.297 1.00 14.82                     ATOM 1113 CG2 THR A 144 0 24.935 24.215 15.104 1.00 15.98                     ATOM 1114 N ILE A 145 0 20.821 26.834 14.898 1.00 13.92                       ATOM 1115 CA ILE A 145 0 19.697 27.550 15.500 1.00 14.31                      ATOM 1116 C ILE A 145 0 18.392 26.835 15.139 1.00 13.84                       ATOM 1117 O ILE A 145 0 18.127 26.478 13.996 1.00 12.32                       ATOM 1118 CB ILE A 145 0 19.641 29.016 15.011 1.00 15.15                      ATOM 1119 CG1 ILE A 145 0 20.881 29.726 15.608 1.00 16.27                     ATOM 1120 CG2 ILE A 145 0 18.346 29.736 15.375 1.00 13.14                     ATOM 1121 CD1 ILE A 145 0 21.256 31.006 14.892 1.00 16.72                     ATOM 1122 N ILE A 146 0 17.550 26.644 16.141 1.00 13.54                       ATOM 1123 CA ILE A 146 0 16.263 25.983 15.926 1.00 13.70                      ATOM 1124 C ILE A 146 0 15.167 26.899 16.494 1.00 12.67                       ATOM 1125 O ILE A 146 0 15.155 27.082 17.714 1.00 10.09                       ATOM 1126 CB ILE A 146 0 16.183 24.580 16.553 1.00 15.97                      ATOM 1127 CG1 ILE A 146 0 17.280 23.621 16.012 1.00 17.29                     ATOM 1128 CG2 ILE A 146 0 14.831 23.937 16.207 1.00 14.52                     ATOM 1129 CD1 ILE A 146 0 17.359 22.340 16.832 1.00 18.45                     ATOM 1130 N THR A 147 0 14.360 27.507 15.610 1.00 10.81                       ATOM 1131 CA THR A 147 0 13.240 28.310 16.102 1.00 12.54                      ATOM 1132 C THR A 147 0 11.912 27.526 15.988 1.00 13.55                       ATOM 1133 O THR A 147 0 11.655 26.724 15.076 1.00 12.65                       ATOM 1134 CB THR A 147 0 13.078 29.642 15.351 1.00 12.37                      ATOM 1135 OG1 THR A 147 0 12.728 29.311 14.005 1.00 10.17                     ATOM 1136 CG2 THR A 147 0 14.381 30.479 15.402 1.00 11.93                     ATOM 1137 N LEU A 148 0 11.062 27.715 16.972 1.00 12.48                       ATOM 1138 CA LEU A 148 0 9.719 27.171 17.039 1.00 13.90                       ATOM 1139 C LEU A 148 0 8.719 28.350 16.916 1.00 15.44                        ATOM 1140 O LEU A 148 0 8.860 29.383 17.579 1.00 15.28                        ATOM 1141 CB LEU A 148 0 9.501 26.419 18.340 1.00 12.83                       ATOM 1142 CG LEU A 148 0 10.502 25.293 18.669 1.00 12.45                      ATOM 1143 CD1 LEU A 148 0 10.154 24.669 19.997 1.00 11.49                     ATOM 1144 CD2 LEU A 148 0 10.552 24.203 17.597 1.00 11.82                     ATOM 1145 N ALA A 149 0 7.726 28.241 16.053 1.00 14.08                        ATOM 1146 CA ALA A 149 0 6.725 29.256 15.825 1.00 15.37                       ATOM 1147 C ALA A 149 0 5.336 28.658 15.521 1.00 16.78                        ATOM 1148 O ALA A 149 0 5.198 27.637 14.841 1.00 15.78                        ATOM 1149 CB ALA A 149 0 7.068 30.127 14.628 1.00 13.22                       ATOM 1150 N ASP A 150 0 4.337 29.344 16.065 1.00 16.39                        ATOM 1151 CA ASP A 150 0 2.941 28.995 15.864 1.00 15.96                       ATOM 1152 C ASP A 150 0 2.515 29.758 14.624 1.00 16.53                        ATOM 1153 O ASP A 150 0 2.960 30.905 14.483 1.00 18.17                        ATOM 1154 CB ASP A 150 0 2.066 29.440 17.027 1.00 16.78                       ATOM 1155 CG ASP A 150 0 2.345 30.836 17.561 1.00 18.15                       ATOM 1156 OD1 ASP A 150 0 3.410 31.472 17.347 1.00 16.29                      ATOM 1157 OD2 ASP A 150 0 1.414 31.311 18.264 1.00 17.83                      ATOM 1158 N TRP A 151 0 1.776 29.157 13.726 1.00 15.62                        ATOM 1159 CA TRP A 151 0 1.366 29.828 12.499 1.00 14.37                       ATOM 1160 C TRP A 151 0 -0.140 29.688 12.226 1.00 14.78                       ATOM 1161 O TRP A 151 0 -0.679 28.607 12.425 1.00 13.41                       ATOM 1162 CB TRP A 151 0 2.229 29.239 11.373 1.00 13.56                       ATOM 1163 CG TRP A 151 0 2.046 30.004 10.097 1.00 13.31                       ATOM 1164 CD1 TRP A 151 0 1.385 29.545 8.991 1.00 13.60                       ATOM 1165 CD2 TRP A 151 0 2.484 31.316 9.806 1.00 15.46                       ATOM 1166 NE1 TRP A 151 0 1.412 30.497 8.017 1.00 14.49                       ATOM 1167 CE2 TRP A 151 0 2.061 31.605 8.473 1.00 15.53                       ATOM 1168 CE3 TRP A 151 0 3.189 32.294 10.522 1.00 16.28                      ATOM 1169 CZ2 TRP A 151 0 2.306 32.822 7.846 1.00 16.57                       ATOM 1170 CZ3 TRP A 151 0 3.436 33.505 9.881 1.00 18.22                       ATOM 1171 CH2 TRP A 151 0 3.003 33.766 8.560 1.00 18.00                       ATOM 1172 N TYR A 152 0 -0.818 30.745 11.812 1.00 15.59                       ATOM 1173 CA TYR A 152 0 -2.266 30.813 11.614 1.00 17.47                      ATOM 1174 C TYR A 152 0 -2.556 31.086 10.149 1.00 18.79                       ATOM 1175 O TYR A 152 0 -1.830 31.856 9.521 1.00 19.15                        ATOM 1176 CB TYR A 152 0 -2.981 31.930 12.434 1.00 16.37                      ATOM 1177 CG TYR A 152 0 -2.539 31.776 13.887 1.00 16.24                      ATOM 1178 CD1 TYR A 152 0 -1.313 32.303 14.318 1.00 15.22                     ATOM 1179 CD2 TYR A 152 0 -3.267 30.998 14.767 1.00 15.29                     ATOM 1180 CE1 TYR A 152 0 -0.889 32.135 15.626 1.00 14.67                     ATOM 1181 CE2 TYR A 152 0 -2.831 30.799 16.054 1.00 16.52                     ATOM 1182 CZ TYR A 152 0 -1.632 31.369 16.474 1.00 16.12                      ATOM 1183 OH TYR A 152 0 -1.219 31.139 17.771 1.00 16.36                      ATOM 1184 N HIS A 153 0 -3.590 30.445 9.599 1.00 20.39                        ATOM 1185 CA HIS A 153 0 -3.899 30.683 8.181 1.00 21.90                       ATOM 1186 C HIS A 153 0 -4.642 31.988 7.952 1.00 21.94                        ATOM 1187 O HIS A 153 0 -4.750 32.386 6.784 1.00 22.32                        ATOM 1188 CB HIS A 153 0 -4.592 29.483 7.549 1.00 22.29                       ATOM 1189 CG HIS A 153 0 -3.651 28.319 7.385 1.00 24.52                       ATOM 1190 ND1 HIS A 153 0 -4.071 27.022 7.258 1.00 24.25                      ATOM 1191 CD2 HIS A 153 0 -2.286 28.274 7.338 1.00 23.32                      ATOM 1192 CE1 HIS A 153 0 -3.034 26.220 7.124 1.00 24.15                      ATOM 1193 NE2 HIS A 153 0 -1.956 26.965 7.178 1.00 24.30                      ATOM 1194 N ILE A 154 0 -5.084 32.718 8.972 1.00 21.86                        ATOM 1195 CA ILE A 154 0 -5.611 34.046 8.686 1.00 24.39                       ATOM 1196 C ILE A 154 0 4.904 35.051 9.597 1.00 22.15                         ATOM 1197 O ILE A 154 0 4.517 34.732 10.698 1.00 20.15                        ATOM 1198 CB ILE A 154 0 -7.120 34.281 8.693 1.00 26.43                       ATOM 1199 CG1 ILE A 154 0 -7.682 34.498 10.099 1.00 27.66                     ATOM 1200 CG2 ILE A 154 0 -7.947 33.251 7.928 1.00 26.60                      ATOM 1201 CD1 ILE A 154 0 -7.312 33.468 11.125 1.00 28.86                     ATOM 1202 N PRO A 155 0 -4.723 36.255 9.105 1.00 23.79                        ATOM 1203 CA PRO A 155 0 -4.108 37.361 9.816 1.00 23.66                       ATOM 1204 C PRO A 155 0 -4.604 37.435 11.252 1.00 24.59                       ATOM 1205 O PRO A 155 0 -5.814 37.317 11.539 1.00 24.53                       ATOM 1206 CB PRO A 155 0 -4.546 38.634 9.077 1.00 24.20                       ATOM 1207 CG PRO A 155 0 -4.990 38.162 7.733 1.00 23.40                       ATOM 1208 CD PRO A 155 0 -5.207 36.672 7.776 1.00 23.41                       ATOM 1209 N ALA A 156 0 -3.704 37.776 12.178 1.00 24.03                       ATOM 1210 CA ALA A 156 0 -4.066 37.806 13.588 1.00 25.45                      ATOM 1211 C ALA A 156 0 -5.262 38.667 13.992 1.00 24.85                       ATOM 1212 O ALA A 156 0 -6.083 38.217 14.798 1.00 22.79                       ATOM 1213 CB ALA A 156 0 -2.866 38.045 14.492 1.00 24.30                      ATOM 1214 N PRO A 157 0 -5.393 39.873 13.518 1.00 25.98                       ATOM 1215 CA PRO A 157 0 -6.521 40.741 13.807 1.00 28.77                      ATOM 1216 C PRO A 157 0 -7.840 40.092 13.406 1.00 30.78                       ATOM 1217 O PRO A 157 0 -8.798 40.416 14.105 1.00 34.62                       ATOM 1218 CB PRO A 157 0 -6.324 42.071 13.068 1.00 26.56                      ATOM 1219 CG PRO A 157 0 -4.859 42.013 12.762 1.00 25.98                      ATOM 1220 CD PRO A 157 0 -4.480 40.547 12.585 1.00 25.96                      ATOM 1221 N SER A 158 0 -7.950 39.207 12.430 1.00 30.95                       ATOM 1222 CA SER A 158 0 -9.174 38.549 12.047 1.00 31.32                      ATOM 1223 C SER A 158 0 -9.450 37.288 12.851 1.00 33.61                       ATOM 1224 O SER A 158 0 -10.472 36.633 12.575 1.00 34.71                      ATOM 1225 CB SER A 158 0 -9.176 38.118 10.577 1.00 30.14                      ATOM 1226 OG SER A 158 0 -8.942 39.187 9.665 1.00 31.20                       ATOM 1227 N ILE A 159 0 -8.588 36.875 13.773 1.00 34.23                       ATOM 1228 CA ILE A 159 0 -8.918 35.642 14.491 1.00 36.40                      ATOM 1229 C ILE A 159 0 -10.189 35.896 15.309 1.00 39.20                      ATOM 1230 O ILE A 159 0 -10.294 36.875 16.046 1.00 39.00                      ATOM 1231 CB ILE A 159 0 -7.769 35.121 15.360 1.00 35.56                      ATOM 1232 CG1 ILE A 159 0 -6.713 34.408 14.485 1.00 35.58                     ATOM 1233 CG2 ILE A 159 0 -8.262 34.184 16.452 1.00 34.97                     ATOM 1234 CD1 ILE A 159 0 -5.388 34.268 15.212 1.00 34.91                     ATOM 1235 N GLN A 160 0 -11.137 34.969 15.196 1.00 41.53                      ATOM 1236 CA GLN A 160 0 -12.398 35.056 15.946 1.00 42.57                     ATOM 1237 C GLN A 160 0 -12.466 33.914 16.949 1.00 40.51                      ATOM 1238 O GLN A 160 0 -12.308 32.741 16.585 1.00 41.96                      ATOM 1239 CB GLN A 160 0 -13.542 35.062 14.937 1.00 45.52                     ATOM 1240 CG GLN A 160 0 -14.814 34.319 15.267 1.00 48.48                     ATOM 1241 CD GLN A 160 0 -15.570 33.799 14.055 1.00 50.12                     ATOM 1242 OE1 GLN A 160 0 -16.204 32.737 14.118 1.00 50.77                    ATOM 1243 NE2 GLN A 160 0 -15.504 34.520 12.940 1.00 51.22                    ATOM 1244 N GLY A 161 0 -12.667 34.191 18.225 1.00 37.10                      ATOM 1245 CA GLY A 161 0 -12.722 33.112 19.208 1.00 34.91                     ATOM 1246 C GLY A 161 0 -11.305 32.826 19.696 1.00 34.13                      ATOM 1247 O GLY A 161 0 -10.412 33.648 19.451 1.00 32.40                      ATOM 1248 N ALA A 162 0 -11.158 31.738 20.433 1.00 33.01                      ATOM 1249 CA ALA A 162 0 -9.864 31.355 20.988 1.00 32.39                      ATOM 1250 C ALA A 162 0 -8.927 30.902 19.880 1.00 31.53                       ATOM 1251 O ALA A 162 0 -9.285 30.132 19.013 1.00 30.73                       ATOM 1252 CB ALA A 162 0 -10.058 30.263 22.010 1.00 34.12                     ATOM 1253 N ALA A 163 0 -7.731 31.475 19.851 1.00 32.06                       ATOM 1254 CA ALA A 163 0 -6.740 31.202 18.814 1.00 30.85                      ATOM 1255 C ALA A 163 0 -6.219 29.774 18.897 1.00 29.40                       ATOM 1256 O ALA A 163 0 -5.967 29.223 19.965 1.00 30.49                       ATOM 1257 CB ALA A 163 0 -5.607 32.217 18.911 1.00 30.29                      ATOM 1258 N GLN A 164 0 -6.101 29.130 17.754 1.00 28.69                       ATOM 1259 CA GLN A 164 0 -5.616 27.769 17.612 1.00 28.24                      ATOM 1260 C GLN A 164 0 -4.720 27.744 16.370 1.00 25.02                       ATOM 1261 O GLN A 164 0 -5.157 28.046 15.260 1.00 23.64                       ATOM 1262 CB GLN A 164 0 -6.732 26.756 17.361 1.00 31.99                      ATOM 1263 CG GLN A 164 0 -7.885 26.640 18.319 1.00 36.24                      ATOM 1264 CD GLN A 164 0 -7.535 25.809 19.540 1.00 40.95                      ATOM 1265 OE1 GLN A 164 0 -7.863 26.166 20.684 1.00 43.34                     ATOM 1266 NE2 GLN A 164 0 -6.864 24.672 19.328 1.00 41.86                     ATOM 1267 N PRO A 165 0 -3.446 27.406 16.549 1.00 22.68                       ATOM 1268 CA PRO A 165 0 -2.501 27.360 15.463 1.00 20.43                      ATOM 1269 C PRO A 165 0 -2.856 26.294 14.429 1.00 18.89                       ATOM 1270 O PRO A 165 0 -3.286 25.176 14.715 1.00 18.00                       ATOM 1271 CB PRO A 165 0 -1.126 27.075 16.088 1.00 20.83                      ATOM 1272 CG PRO A 165 0 -1.476 26.651 17.479 1.00 22.05                      ATOM 1273 CD PRO A 165 0 -2.873 27.081 17.851 1.00 21.57                      ATOM 1274 N ASP A 166 0 -2.667 26.608 13.169 1.00 17.50                       ATOM 1275 CA ASP A 166 0 -2.829 25.677 12.059 1.00 19.82                      ATOM 1276 C ASP A 166 0 -1.591 24.788 11.930 1.00 19.47                       ATOM 1277 O ASP A 166 0 -1.692 23.649 11.506 1.00 19.38                       ATOM 1278 CB ASP A 166 0 -3.005 26.413 10.727 1.00 19.75                      ATOM 1279 CG ASP A 166 0 -4.347 27.162 10.728 1.00 21.69                      ATOM 1280 OD1 ASP A 166 0 -5.376 26.480 10.593 1.00 22.24                     ATOM 1281 OD2 ASP A 166 0 -4.384 28.392 10.885 1.00 22.13                     ATOM 1282 N ALA A 167 0 -0.435 25.386 12.231 1.00 18.54                       ATOM 1283 CA ALA A 167 0 0.806 24.614 12.142 1.00 18.74                       ATOM 1284 C ALA A 167 0 1.867 25.056 13.148 1.00 17.69                        ATOM 1285 O ALA A 167 0 1.874 26.147 13.715 1.00 15.83                        ATOM 1286 CB ALA A 167 0 1.387 24.767 10.735 1.00 17.32                       ATOM 1287 N THR A 168 0 2.826 24.166 13.335 1.00 18.40                        ATOM 1288 CA THR A 168 0 4.087 24.402 14.027 1.00 14.85                       ATOM 1289 C THR A 168 0 5.180 24.553 12.955 1.00 15.24                        ATOM 1290 O THR A 168 0 5.402 23.737 12.071 1.00 12.99                        ATOM 1291 CB THR A 168 0 4.530 23.235 14.900 1.00 14.31                       ATOM 1292 OG1 THR A 168 0 3.558 23.068 15.920 1.00 12.30                      ATOM 1293 CG2 THR A 168 0 5.921 23.516 15.524 1.00 13.60                      ATOM 1294 N LEU A 169 0 5.867 25.686 12.973 1.00 16.69                        ATOM 1295 CA LEU A 169 0 6.976 26.002 12.071 1.00 14.74                       ATOM 1296 C LEU A 169 0 8.285 25.747 12.833 1.00 14.34                        ATOM 1297 O LEU A 169 0 8.497 26.259 13.942 1.00 12.34                        ATOM 1298 CB LEU A 169 0 6.890 27.471 11.652 1.00 14.90                       ATOM 1299 CG LEU A 169 0 6.071 27.845 10.428 1.00 17.83                       ATOM 1300 CD1 LEU A 169 0 4.978 26.825 10.133 1.00 15.89                      ATOM 1301 CD2 LEU A 169 0 5.500 29.254 10.443 1.00 16.43                      ATOM 1302 N ILE A 170 0 9.141 24.923 12.255 1.00 14.06                        ATOM 1303 CA ILE A 170 0 10.472 24.659 12.819 1.00 14.01                      ATOM 1304 C ILE A 170 0 11.397 25.312 11.784 1.00 15.19                       ATOM 1305 O ILE A 170 0 11.307 25.009 10.585 1.00 14.73                       ATOM 1306 CB ILE A 170 0 10.807 23.179 13.025 1.00 14.75                      ATOM 1307 CG1 ILE A 170 0 9.849 22.605 14.069 1.00 13.74                      ATOM 1308 CG2 ILE A 170 0 12.268 22.983 13.468 1.00 13.47                     ATOM 1309 CD1 ILE A 170 0 9.915 21.134 14.385 1.00 15.26                      ATOM 1310 N ASN A 171 0 12.166 26.317 12.208 1.00 13.13                       ATOM 1311 CA ASN A 171 0 12.992 27.042 11.250 1.00 13.74                      ATOM 1312 C ASN A 171 0 12.163 27.517 10.083 1.00 13.71                       ATOM 1313 O ASN A 171 0 12.562 27.381 8.921 1.00 13.20                        ATOM 1314 CB ASN A 171 0 14.220 26.209 10.793 1.00 14.42                      ATOM 1315 CG ASN A 171 0 15.236 26.157 11.940 1.00 16.29                      ATOM 1316 OD1 ASN A 171 0 15.123 26.983 12.875 1.00 16.78                     ATOM 1317 ND2 ASN A 171 0 16.203 25.259 11.964 1.00 14.32                     ATOM 1318 N GLY A 172 0 10.967 28.074 10.337 1.00 14.17                       ATOM 1319 CA GLY A 172 0 10.157 28.619 9.270 1.00 11.74                       ATOM 1320 C GLY A 172 0 9.387 27.636 8.433 1.00 14.40                         ATOM 1321 O GLY A 172 0 8.783 28.064 7.441 1.00 15.60                         ATOM 1322 N LYS A 173 0 9.430 26.319 8.669 1.00 13.84                         ATOM 1323 CA LYS A 173 0 8.777 25.363 7.794 1.00 13.67                        ATOM 1324 C LYS A 173 0 8.038 24.303 8.589 1.00 13.59                         ATOM 1325 O LYS A 173 0 8.445 24.027 9.723 1.00 11.70                         ATOM 1326 CB LYS A 173 0 9.775 24.645 6.875 1.00 17.03                        ATOM 1327 CG LYS A 173 0 10.704 25.577 6.118 1.00 17.63                       ATOM 1328 CD LYS A 173 0 11.508 24.796 5.094 1.00 20.84                       ATOM 1329 CE LYS A 173 0 12.213 25.821 4.198 1.00 22.63                       ATOM 1330 NZ LYS A 173 0 13.304 25.087 3.499 1.00 28.08                       ATOM 1331 N GLY A 174 0 6.922 23.821 8.014 1.00 12.28                         ATOM 1332 CA GLY A 174 0 6.178 22.768 8.753 1.00 11.45                        ATOM 1333 C GLY A 174 0 4.958 22.409 7.896 1.00 13.55                         ATOM 1334 O GLY A 174 0 4.823 22.877 6.760 1.00 13.37                         ATOM 1335 N ARG A 175 0 4.042 21.619 8.432 1.00 14.54                         ATOM 1336 CA ARG A 175 0 2.859 21.201 7.687 1.00 16.62                        ATOM 1337 C ARG A 175 0 1.598 21.336 8.541 1.00 17.67                         ATOM 1338 O ARG A 175 0 1.727 21.264 9.769 1.00 18.41                         ATOM 1339 CB ARG A 175 0 2.985 19.718 7.292 1.00 16.05                        ATOM 1340 CG ARG A 175 0 3.894 19.472 6.116 1.00 16.55                        ATOM 1341 CD ARG A 175 0 4.358 18.009 6.108 1.00 17.70                        ATOM 1342 NE ARG A 175 0 5.421 17.861 5.097 1.00 17.74                        ATOM 1343 CZ ARG A 175 0 5.971 16.667 4.792 1.00 17.63                        ATOM 1344 NH1 ARG A 175 0 6.918 16.665 3.866 1.00 17.25                       ATOM 1345 NH2 ARG A 175 0 5.594 15.538 5.375 1.00 14.80                       ATOM 1346 N TYR A 176 0 0.429 21.438 7.908 1.00 18.08                         ATOM 1347 CA TYR A 176 0 -0.800 21.481 8.746 1.00 18.67                       ATOM 1348 C TYR A 176 0 -1.613 20.200 8.509 1.00 18.24                        ATOM 1349 O TYR A 176 0 -1.417 19.534 7.483 1.00 17.67                        ATOM 1350 CB TYR A 176 0 -1.635 22.709 8.462 1.00 17.21                       ATOM 1351 CG TYR A 176 0 -2.102 22.931 7.053 1.00 16.36                       ATOM 1352 CD1 TYR A 176 0 -1.246 23.433 6.089 1.00 14.84                      ATOM 1353 CD2 TYR A 176 0 -3.441 22.676 6.677 1.00 17.26                      ATOM 1354 CE1 TYR A 176 0 -1.640 23.686 4.796 1.00 16.01                      ATOM 1355 CE2 TYR A 176 0 -3.862 22.908 5.361 1.00 16.65                      ATOM 1356 CZ TYR A 176 0 -2.967 23.407 4.432 1.00 17.65                       ATOM 1357 OH TYR A 176 0 -3.347 23.678 3.131 1.00 17.81                       ATOM 1358 N VAL A 177 0 -2.427 19.815 9.464 1.00 18.46                        ATOM 1359 CA VAL A 177 0 -3.200 18.571 9.303 1.00 21.18                       ATOM 1360 C VAL A 177 0 -4.090 18.639 8.073 1.00 21.50                        ATOM 1361 O VAL A 177 0 -4.788 19.620 7.858 1.00 21.85                        ATOM 1362 CB VAL A 177 0 -4.072 18.306 10.532 1.00 22.29                      ATOM 1363 CG1 VAL A 177 0 -4.802 16.974 10.370 1.00 21.70                     ATOM 1364 CG2 VAL A 177 0 -3.205 18.289 11.784 1.00 22.43                     ATOM 1365 N GLY A 178 0 -3.989 17.707 7.142 1.00 21.84                        ATOM 1366 CA GLY A 178 0 -4.761 17.742 5.918 1.00 20.35                       ATOM 1367 C GLY A 178 0 -4.047 18.602 4.900 1.00 22.84                        ATOM 1368 O GLY A 178 0 -4.576 18.673 3.774 1.00 23.86                        ATOM 1369 N GLY A 179 0 -2.887 19.220 5.210 1.00 21.49                        ATOM 1370 CA GLY A 179 0 -2.291 20.060 4.149 1.00 19.94                       ATOM 1371 C GLY A 179 0 -1.389 19.250 3.242 1.00 18.86                        ATOM 1372 O GLY A 179 0 -1.192 18.052 3.399 1.00 19.35                        ATOM 1373 N PRO A 180 0 -0.800 19.905 2.268 1.00 19.42                        ATOM 1374 CA PRO A 180 0 0.150 19.328 1.335 1.00 19.92                        ATOM 1375 C PRO A 180 0 1.430 18.922 2.041 1.00 20.56                         ATOM 1376 O PRO A 180 0 1.731 19.399 3.145 1.00 20.66                         ATOM 1377 CB PRO A 180 0 0.503 20.399 0.298 1.00 19.52                        ATOM 1378 CG PRO A 180 0 -0.144 21.639 0.829 1.00 19.70                       ATOM 1379 CD PRO A 180 0 -0.930 21.356 2.081 1.00 19.79                       ATOM 1380 N ALA A 181 0 2.213 18.059 1.403 1.00 21.19                         ATOM 1381 CA ALA A 181 0 3.489 17.644 2.007 1.00 23.04                        ATOM 1382 C ALA A 181 0 4.548 18.723 1.772 1.00 21.24                         ATOM 1383 O ALA A 181 0 5.465 18.522 0.986 1.00 23.93                         ATOM 1384 CB ALA A 181 0 3.928 16.305 1.435 1.00 21.73                        ATOM 1385 N ALA A 182 0 4.398 19.905 2.315 1.00 19.30                         ATOM 1386 CA ALA A 182 0 5.357 20.987 2.183 1.00 18.39                        ATOM 1387 C ALA A 182 0 6.706 20.549 2.791 1.00 17.36                         ATOM 1388 O ALA A 182 0 6.858 19.712 3.701 1.00 16.16                         ATOM 1389 CB ALA A 182 0 4.826 22.209 2.932 1.00 17.68                        ATOM 1390 N GLU A 183 0 7.739 21.103 2.210 1.00 18.23                         ATOM 1391 CA GLU A 183 0 9.134 20.882 2.599 1.00 20.90                        ATOM 1392 C GLU A 183 0 9.381 21.078 4.093 1.00 18.87                         ATOM 1393 O GLU A 183 0 8.976 22.073 4.699 1.00 17.80                         ATOM 1394 CB GLU A 183 0 9.990 21.875 1.820 1.00 25.16                        ATOM 1395 CG GLU A 183 0 11.508 21.760 1.962 1.00 31.31                       ATOM 1396 CD GLU A 183 0 12.075 22.803 0.998 1.00 34.38                       ATOM 1397 OE1 GLU A 183 0 11.901 22.609 -0.229 1.00 36.88                     ATOM 1398 OE2 GLU A 183 0 12.619 23.809 1.484 1.00 36.18                      ATOM 1399 N LEU A 184 0 10.010 20.093 4.691 1.00 17.33                        ATOM 1400 CA LEU A 184 0 10.388 20.155 6.098 1.00 18.77                       ATOM 1401 C LEU A 184 0 11.780 20.743 6.255 1.00 19.44                        ATOM 1402 O LEU A 184 0 12.582 20.687 5.314 1.00 20.95                        ATOM 1403 CB LEU A 184 0 10.331 18.735 6.673 1.00 18.11                       ATOM 1404 CG LEU A 184 0 8.915 18.125 6.577 1.00 19.10                        ATOM 1405 CD1 LEU A 184 0 8.887 16.734 7.178 1.00 18.87                       ATOM 1406 CD2 LEU A 184 0 7.868 19.026 7.229 1.00 18.69                       ATOM 1407 N SER A 185 0 12.054 21.342 7.398 1.00 18.46                        ATOM 1408 CA SER A 185 0 13.366 21.883 7.699 1.00 17.73                       ATOM 1409 C SER A 185 0 14.298 20.699 8.018 1.00 16.95                        ATOM 1410 O SER A 185 0 13.883 19.710 8.629 1.00 15.84                        ATOM 1411 CB SER A 185 0 13.303 22.786 8.934 1.00 17.34                       ATOM 1412 OG SER A 185 0 12.846 24.073 8.560 1.00 18.09                       ATOM 1413 N ILE A 186 0 15.533 20.845 7.587 1.00 16.43                        ATOM 1414 CA ILE A 186 0 16.595 19.858 7.821 1.00 16.85                       ATOM 1415 C ILE A 186 0 17.725 20.491 8.626 1.00 15.86                        ATOM 1416 O ILE A 186 0 18.178 21.605 8.387 1.00 11.67                        ATOM 1417 CB ILE A 186 0 17.193 19.390 6.471 1.00 18.77                       ATOM 1418 CG1 ILE A 186 0 16.048 18.895 5.557 1.00 19.78                      ATOM 1419 CG2 ILE A 186 0 18.167 18.241 6.697 1.00 18.53                      ATOM 1420 CD1 ILE A 186 0 16.44 18.731 4.110 1.00 22.35                       ATOM 1421 N VAL A 187 0 18.114 19.840 9.703 1.00 16.18                        ATOM 1422 CA VAL A 187 0 19.243 20.287 10.505 1.00 16.63                      ATOM 1423 C VAL A 187 0 20.362 19.239 10.231 1.00 17.36                       ATOM 1424 O VAL A 187 0 20.158 18.046 10.505 1.00 15.19                       ATOM 1425 CB VAL A 187 0 18.928 20.323 11.984 1.00 16.68                      ATOM 1426 CG1 VAL A 187 0 20.198 20.622 12.796 1.00 16.82                     ATOM 1427 CG2 VAL A 187 0 17.874 21.375 12.275 1.00 17.07                     ATOM 1428 N ASN A 188 0 21.449 19.695 9.634 1.00 16.45                        ATOM 1429 CA ASN A 188 0 22.528 18.766 9.272 1.00 19.84                       ATOM 1430 C ASN A 188 0 23.598 18.597 10.349 1.00 19.41                       ATOM 1431 O ASN A 188 0 24.051 19.618 10.862 1.00 21.31                       ATOM 1432 CB ASN A 188 0 23.209 19.246 7.976 1.00 18.78                       ATOM 1433 CG ASN A 188 0 22.249 19.186 6.797 1.00 20.77                       ATOM 1434 OD1 ASN A 188 0 21.734 20.201 6.305 1.00 21.70                      ATOM 1435 ND2 ASN A 188 0 21.995 17.985 6.286 1.00 20.52                      ATOM 1436 N VAL A 189 0 24.024 17.389 10.681 1.00 17.35                       ATOM 1437 CA VAL A 189 0 25.098 17.164 11.617 1.00 17.93                      ATOM 1438 C VAL A 189 0 26.091 16.135 11.046 1.00 19.82                       ATOM 1439 O VAL A 189 0 25.773 15.392 10.109 1.00 18.90                       ATOM 1440 CB VAL A 189 0 24.660 16.684 13.009 1.00 18.43                      ATOM 1441 CG1 VAL A 189 0 23.931 17.796 13.766 1.00 18.89                     ATOM 1442 CG2 VAL A 189 0 23.760 15.449 12.965 1.00 15.94                     ATOM 1443 N GLU A 190 0 27.242 15.993 11.688 1.00 21.48                       ATOM 1444 CA GLU A 190 0 28.220 14.972 11.274 1.00 24.63                      ATOM 1445 C GLU A 190 0 28.514 14.065 12.469 1.00 23.06                       ATOM 1446 O GLU A 190 0 28.797 14.650 13.522 1.00 21.04                       ATOM 1447 CB GLU A 190 0 29.569 15.551 10.860 1.00 26.79                      ATOM 1448 CG GLU A 190 0 29.571 16.355 9.567 1.00 32.24                       ATOM 1449 CD GLU A 190 0 30.951 16.990 9.351 1.00 34.67                       ATOM 1450 OE1 GLU A 190 0 31.927 16.199 9.305 1.00 35.41                      ATOM 1451 OE2 GLU A 190 0 30.999 18.236 9.264 1.00 35.78                      ATOM 1452 N GLN A 191 0 28.490 12.752 12.256 1.00 21.94                       ATOM 1453 CA GLN A 191 0 28.768 11.824 13.357 1.00 21.92                      ATOM 1454 C GLN A 191 0 30.121 12.151 13.984 1.00 22.68                       ATOM 1455 O GLN A 191 0 31.052 12.516 13.251 1.00 23.08                       ATOM 1456 CB GLN A 191 0 28.797 10.400 12.820 1.00 22.01                      ATOM 1457 CG GLN A 191 0 28.795 9.347 13.917 1.00 23.87                       ATOM 1458 CD GLN A 191 0 28.846 7.966 13.259 1.00 26.64                       ATOM 1459 OE1 GLN A 191 0 29.745 7.761 12.427 1.00 28.86                      ATOM 1460 NE2 GLN A 191 0 27.909 7.080 13.563 1.00 26.40                      ATOM 1461 N GLY A 192 0 30.224 12.119 15.290 1.00 21.84                       ATOM 1462 CA GLY A 192 0 31.418 12.469 15.996 1.00 22.91                      ATOM 1463 C GLY A 192 0 31.564 13.910 16.446 1.00 23.87                       ATOM 1464 O GLY A 192 0 32.394 14.174 17.322 1.00 25.80                       ATOM 1465 N LYS A 193 0 30.839 14.867 15.922 1.00 23.54                       ATOM 1466 CA LYS A 193 0 30.899 16.259 16.362 1.00 22.84                      ATOM 1467 C LYS A 193 0 29.840 16.584 17.404 1.00 21.67                       ATOM 1468 O LYS A 193 0 28.826 15.882 17.538 1.00 20.99                       ATOM 1469 CB LYS A 193 0 30.682 17.155 15.143 1.00 24.53                      ATOM 1470 CG LYS A 193 0 31.900 17.149 14.217 1.00 27.82                      ATOM 1471 CD LYS A 193 0 31.739 18.261 13.199 1.00 30.02                      ATOM 1472 CE LYS A 193 0 33.060 19.001 12.990 1.00 31.93                      ATOM 1473 NZ LYS A 193 0 33.392 18.906 11.540 1.00 33.14                      ATOM 1474 N LYS A 194 0 30.067 17.626 18.169 1.00 19.25                       ATOM 1475 CA LYS A 194 0 29.168 18.115 19.187 1.00 19.49                      ATOM 1476 C LYS A 194 0 28.722 19.523 18.780 1.00 19.40                       ATOM 1477 O LYS A 194 0 29.512 20.285 18.235 1.00 19.29                       ATOM 1478 CB LYS A 194 0 29.771 18.115 20.576 1.00 21.88                      ATOM 1479 CG LYS A 194 0 30.338 16.748 20.999 1.00 25.59                      ATOM 1480 CD LYS A 194 0 31.054 16.902 22.331 1.00 29.48                      ATOM 1481 CE LYS A 194 0 31.455 15.582 22.970 1.00 33.58                      ATOM 1482 NZ LYS A 194 0 30.363 15.049 23.868 1.00 35.93                      ATOM 1483 N TYR A 195 0 27.418 19.818 18.910 1.00 16.92                       ATOM 1484 CA TYR A 195 0 26.858 21.068 18.431 1.00 15.60                      ATOM 1485 C TYR A 195 0 26.143 21.838 19.530 1.00 14.20                       ATOM 1486 O TYR A 195 0 25.394 21.232 20.295 1.00 13.75                       ATOM 1487 CB TYR A 195 0 25.814 20.880 17.300 1.00 16.13                      ATOM 1488 CG TYR A 195 0 26.424 20.225 16.066 1.00 15.41                      ATOM 1489 CD1 TYR A 195 0 26.663 18.851 16.091 1.00 15.91                     ATOM 1490 CD2 TYR A 195 0 26.786 20.942 14.945 1.00 14.73                     ATOM 1491 CE1 TYR A 195 0 27.244 18.204 15.010 1.00 16.55                     ATOM 1492 CE2 TYR A 195 0 27.331 20.312 13.839 1.00 15.60                     ATOM 1493 CZ TYR A 195 0 27.570 18.947 13.888 1.00 16.18                      ATOM 1494 OH TYR A 195 0 28.144 18.287 12.831 1.00 15.64                      ATOM 1495 N ARG A 196 0 26.366 23.136 19.561 1.00 12.74                       ATOM 1496 CA ARG A 196 0 25.619 23.980 20.482 1.00 13.63                      ATOM 1497 C ARG A 196 0 24.343 24.369 19.711 1.00 13.86                       ATOM 1498 O ARG A 196 0 24.343 25.218 18.802 1.00 13.81                       ATOM 1499 CB ARG A 196 0 26.379 25.187 20.991 1.00 13.96                      ATOM 1500 CG ARG A 196 0 25.520 26.162 21.796 1.00 14.22                      ATOM 1501 CD ARG A 196 0 26.337 27.238 22.438 1.00 15.27                      ATOM 1502 NE ARG A 196 0 25.649 28.138 23.319 1.00 17.38                      ATOM 1503 CZ ARG A 196 0 26.203 29.034 24.140 1.00 18.86                      ATOM 1504 NH1 ARG A 196 0 27.540 29.141 24.217 1.00 16.30                     ATOM 1505 NH2 ARG A 196 0 25.377 29.788 24.869 1.00 16.73                     ATOM 1506 N MET A 197 0 23.266 23.624 20.002 1.00 13.86                       ATOM 1507 CA MET A 197 0 21.980 23.932 19.340 1.00 12.98                      ATOM 1508 C MET A 197 0 21.293 25.055 20.127 1.00 12.50                       ATOM 1509 O MET A 197 0 21.285 24.997 21.359 1.00 13.93                       ATOM 1510 CB MET A 197 0 21.118 22.693 19.266 1.00 12.50                      ATOM 1511 CG MET A 197 0 21.762 21.567 18.447 1.00 13.94                      ATOM 1512 SD MET A 197 0 21.860 22.033 16.735 1.00 16.62                      ATOM 1513 CE MET A 197 0 22.157 20.467 15.927 1.00 16.37                      ATOM 1514 N ARG A 198 0 20.768 26.064 19.450 1.00 11.00                       ATOM 1515 CA ARG A 198 0 20.131 27.191 20.137 1.00 11.83                      ATOM 1516 C ARG A 198 0 18.624 27.130 19.868 1.00 12.36                       ATOM 1517 O ARG A 198 0 18.145 27.304 18.731 1.00 10.03                       ATOM 1518 CB ARG A 198 0 20.804 28.460 19.629 1.00 13.98                      ATOM 1519 CG ARG A 198 0 22.282 28.567 20.065 1.00 16.25                      ATOM 1520 CD ARG A 198 0 22.932 29.863 19.626 1.00 16.68                      ATOM 1521 NE ARG A 198 0 24.350 29.957 20.042 1.00 16.91                      ATOM 1522 CZ ARG A 198 0 24.812 30.691 21.055 1.00 15.76                      ATOM 1523 NH1 ARG A 198 0 24.031 31.456 21.820 1.00 13.44                     ATOM 1524 NH2 ARG A 198 0 26.123 30.721 21.316 1.00 15.41                     ATOM 1525 N LEU A 199 0 17.871 26.807 20.908 1.00 10.44                       ATOM 1526 CA LEU A 199 0 16.426 26.568 20.708 1.00 10.69                      ATOM 1527 C LEU A 199 0 15.598 27.772 21.169 1.00 10.07                       ATOM 1528 O LEU A 199 0 15.682 28.216 22.317 1.00 10.07                       ATOM 1529 CB LEU A 199 0 16.003 25.317 21.491 1.00 8.67                       ATOM 1530 CG LEU A 199 0 14.499 24.942 21.391 1.00 10.33                      ATOM 1531 CD1 LEU A 199 0 14.193 24.333 20.023 1.00 8.13                      ATOM 1532 CD2 LEU A 199 0 14.170 23.907 22.485 1.00 9.10                      ATOM 1533 N ILE A 200 0 14.857 28.370 20.242 1.00 10.46                       ATOM 1534 CA ILE A 200 0 14.104 29.572 20.585 1.00 11.72                      ATOM 1535 C ILE A 200 0 12.627 29.428 20.310 1.00 13.84                       ATOM 1536 O ILE A 200 0 12.254 29.059 19.192 1.00 13.22                       ATOM 1537 CB ILE A 200 0 14.628 30.755 19.735 1.00 12.89                      ATOM 1538 CG1 ILE A 200 0 16.165 30.899 19.824 1.00 12.38                     ATOM 1539 CG2 ILE A 200 0 13.998 32.091 20.065 1.00 13.13                     ATOM 1540 CD1 ILE A 200 0 16.811 31.634 18.671 1.00 12.54                     ATOM 1541 N SER A 201 0 11.829 29.825 21.312 1.00 14.64                       ATOM 1542 CA SER A 201 0 10.379 29.849 21.023 1.00 13.89                      ATOM 1543 C SER A 201 0 10.018 31.280 20.608 1.00 11.10                       ATOM 1544 O SER A 201 0 10.250 32.261 21.320 1.00 8.85                        ATOM 1545 CB SER A 201 0 9.539 29.367 22.202 1.00 13.01                       ATOM 1546 OG SER A 201 0 8.313 30.047 22.207 1.00 12.19                       ATOM 1547 N LEU A 202 0 9.428 31.376 19.438 1.00 9.64                         ATOM 1548 CA LEU A 202 0 8.959 32.637 18.881 1.00 9.06                        ATOM 1549 C LEU A 202 0 7.415 32.740 19.046 1.00 10.40                        ATOM 1550 O LEU A 202 0 6.802 33.528 18.351 1.00 9.36                         ATOM 1551 CB LEU A 202 0 9.239 32.618 17.379 1.00 9.09                        ATOM 1552 CG LEU A 202 0 10.691 32.451 16.888 1.00 10.90                      ATOM 1553 CD1 LEU A 202 0 10.637 32.470 15.367 1.00 10.05                     ATOM 1554 CD2 LEU A 202 0 11.617 33.559 17.414 1.00 8.56                      ATOM 1555 N SER A 203 0 6.821 31.942 19.892 1.00 9.59                         ATOM 1556 CA SER A 203 0 5.414 31.756 20.017 1.00 15.31                       ATOM 1557 C SER A 203 0 4.624 32.960 20.544 1.00 16.67                        ATOM 1558 O SER A 203 0 4.964 33.676 21.483 1.00 16.42                        ATOM 1559 CB SER A 203 0 5.130 30.505 20.867 1.00 15.21                       ATOM 1560 OG SER A 203 0 3.742 30.240 21.004 1.00 17.14                       ATOM 1561 N CYS A 204 0 3.428 33.051 19.984 1.00 17.18                        ATOM 1562 CA CYS A 204 0 2.442 34.018 20.470 1.00 18.43                       ATOM 1563 C CYS A 204 0 1.599 33.316 21.522 1.00 17.02                        ATOM 1564 O CYS A 204 0 0.867 34.039 22.200 1.00 17.27                        ATOM 1565 CB CYS A 204 0 1.524 34.508 19.334 1.00 18.60                       ATOM 1566 SG CYS A 204 0 2.135 36.038 18.612 1.00 20.23                       ATOM 1567 N ASP A 205 0 1.687 31.989 21.665 1.00 16.38                        ATOM 1568 CA ASP A 205 0 0.776 31.392 22.683 1.00 12.26                       ATOM 1569 C ASP A 205 0 1.123 30.002 23.087 1.00 11.34                        ATOM 1570 O ASP A 205 0 1.432 29.687 24.255 1.00 11.40                        ATOM 1571 CB ASP A 205 0 -0.622 31.516 22.076 1.00 14.87                      ATOM 1572 CG ASP A 205 0 -1.729 30.881 22.892 1.00 16.61                      ATOM 1573 OD1 ASP A 205 0 -2.884 30.999 22.433 1.00 18.48                     ATOM 1574 OD2 ASP A 205 0 -1.534 30.263 23.966 1.00 17.48                     ATOM 1575 N PRO A 206 0 1.036 29.030 22.205 1.00 11.79                        ATOM 1576 CA PRO A 206 0 1.313 27.639 22.542 1.00 11.91                       ATOM 1577 C PRO A 206 0 2.739 27.411 23.045 1.00 14.01                        ATOM 1578 O PRO A 206 0 3.676 28.135 22.661 1.00 14.38                        ATOM 1579 CB PRO A 206 0 1.124 26.816 21.262 1.00 11.87                       ATOM 1580 CG PRO A 206 0 1.112 27.893 20.191 1.00 12.83                       ATOM 1581 CD PRO A 206 0 0.749 29.241 20.766 1.00 11.09                       ATOM 1582 N ASN A 207 0 2.888 26.439 23.911 1.00 13.06                        ATOM 1583 CA ASN A 207 0 4.128 25.919 24.429 1.00 15.01                       ATOM 1584 C ASN A 207 0 4.332 24.591 23.677 1.00 15.84                        ATOM 1585 O ASN A 207 0 3.376 24.095 23.038 1.00 16.22                        ATOM 1586 CB ASN A 207 0 4.144 25.682 25.933 1.00 15.12                       ATOM 1587 CG ASN A 207 0 3.054 24.708 26.395 1.00 19.36                       ATOM 1588 OD1 ASN A 207 0 2.062 25.161 27.014 1.00 19.36                      ATOM 1589 ND2 ASN A 207 0 3.174 23.408 26.203 1.00 16.49                      ATOM 1590 N TRP A 208 0 5.557 24.077 23.634 1.00 14.46                        ATOM 1591 CA TRP A 208 0 5.827 22.865 22.892 1.00 12.04                       ATOM 1592 C TRP A 208 0 6.638 21.921 23.783 1.00 13.85                        ATOM 1593 O TRP A 208 0 7.482 22.385 24.558 1.00 13.02                        ATOM 1594 CB TRP A 208 0 6.654 23.136 21.628 1.00 11.91                       ATOM 1595 CG TRP A 208 0 5.951 23.769 20.465 1.00 11.27                       ATOM 1596 CD1 TRP A 208 0 5.149 23.164 19.561 1.00 10.33                      ATOM 1597 CD2 TRP A 208 0 5.988 25.158 20.092 1.00 10.29                      ATOM 1598 NE1 TRP A 208 0 4.698 24.078 18.625 1.00 10.91                      ATOM 1599 CE2 TRP A 208 0 5.201 25.313 18.954 1.00 9.64                       ATOM 1600 CE3 TRP A 208 0 6.634 26.294 20.625 1.00 10.25                      ATOM 1601 CZ2 TRP A 208 0 5.011 26.553 18.344 1.00 8.53                       ATOM 1602 CZ3 TRP A 208 0 6.494 27.514 20.019 1.00 10.02                      ATOM 1603 CH2 TRP A 208 0 5.668 27.633 18.881 1.00 11.79                      ATOM 1604 N GLN A 209 0 6.420 20.620 23.580 1.00 13.82                        ATOM 1605 CA GLN A 209 0 7.240 19.588 24.192 1.00 13.83                       ATOM 1606 C GLN A 209 0 8.251 19.281 23.075 1.00 13.07                        ATOM 1607 O GLN A 209 0 7.848 18.968 21.948 1.00 14.18                        ATOM 1608 CB GLN A 209 0 6.441 18.319 24.487 1.00 15.65                       ATOM 1609 CG GLN A 209 0 5.449 18.481 25.649 1.00 17.26                       ATOM 1610 CD GLN A 209 0 6.177 18.514 26.975 1.00 18.17                       ATOM 1611 OE1 GLN A 209 0 7.414 18.471 27.002 1.00 20.00                      ATOM 1612 NE2 GLN A 209 0 5.462 18.570 28.085 1.00 16.89                      ATOM 1613 N PHE A 210 0 9.538 19.461 23.351 1.00 11.26                        ATOM 1614 CA PHE A 210 0 10.526 19.329 22.287 1.00 10.01                      ATOM 1615 C PHE A 210 0 11.457 18.153 22.585 1.00 9.18                        ATOM 1616 O PHE A 210 0 11.894 17.999 23.732 1.00 10.07                       ATOM 1617 CB PHE A 210 0 11.370 20.629 22.292 1.00 10.86                      ATOM 1618 CG PHE A 210 0 12.489 20.581 21.292 1.00 9.63                       ATOM 1619 CD1 PHE A 210 0 13.760 20.179 21.674 1.00 9.95                      ATOM 1620 CD2 PHE A 210 0 12.251 20.922 19.984 1.00 8.54                      ATOM 1621 CE1 PHE A 210 0 14.778 20.150 20.738 1.00 9.23                      ATOM 1622 CE2 PHE A 210 0 13.243 20.862 19.023 1.00 7.93                      ATOM 1623 CZ PHE A 210 0 14.520 20.491 19.426 1.00 8.71                       ATOM 1624 N SER A 211 0 11.741 17.384 21.545 1.00 8.62                        ATOM 1625 CA SER A 211 0 12.645 16.255 21.716 1.00 10.71                      ATOM 1626 C SER A 211 0 13.142 15.844 20.347 1.00 11.36                       ATOM 1627 O SER A 211 0 12.661 16.323 19.315 1.00 9.99                        ATOM 1628 CB SER A 211 0 11.970 15.070 22.427 1.00 10.56                      ATOM 1629 OG SER A 211 0 10.899 14.731 21.513 1.00 12.92                      ATOM 1630 N ILE A 212 0 14.268 15.122 20.390 1.00 13.67                       ATOM 1631 CA ILE A 212 0 14.883 14.680 19.131 1.00 14.79                      ATOM 1632 C ILE A 212 0 15.013 13.166 19.220 1.00 15.44                       ATOM 1633 O ILE A 212 0 15.624 12.689 20.177 1.00 15.98                       ATOM 1634 CB ILE A 212 0 16.255 15.341 18.887 1.00 17.04                      ATOM 1635 CG1 ILE A 212 0 16.082 16.859 18.756 1.00 15.64                     ATOM 1636 CG2 ILE A 212 0 16.935 14.722 17.648 1.00 15.24                     ATOM 1637 CD1 ILE A 212 0 17.352 17.648 18.553 1.00 16.57                     ATOM 1638 N ASP A 213 0 14.453 12.418 18.281 1.00 15.53                       ATOM 1639 CA ASP A 213 0 14.549 10.952 18.401 1.00 16.50                      ATOM 1640 C ASP A 213 0 16.004 10.469 18.541 1.00 16.69                       ATOM 1641 O ASP A 213 0 16.948 10.902 17.851 1.00 14.36                       ATOM 1642 CB ASP A 213 0 13.884 10.359 17.173 1.00 17.15                      ATOM 1643 CG ASP A 213 0 12.369 10.467 17.144 1.00 18.12                      ATOM 1644 OD1 ASP A 213 0 11.751 10.995 18.092 1.00 16.90                     ATOM 1645 OD2 ASP A 213 0 11.801 9.990 16.129 1.00 17.35                      ATOM 1646 N GLY A 214 0 16.198 9.559 19.477 1.00 15.76                        ATOM 1647 CA GLY A 214 0 17.457 8.900 19.747 1.00 17.22                       ATOM 1648 C GLY A 214 0 18.548 9.757 20.368 1.00 18.54                        ATOM 1649 O GLY A 214 0 19.680 9.277 20.404 1.00 18.20                        ATOM 1650 N HIS A 215 0 18.341 11.024 20.738 1.00 18.17                       ATOM 1651 CA HIS A 215 0 19.422 11.880 21.229 1.00 17.59                      ATOM 1652 C HIS A 215 0 19.096 12.505 22.577 1.00 17.92                       ATOM 1653 O HIS A 215 0 17.917 12.696 22.898 1.00 20.45                       ATOM 1654 CB HIS A 215 0 19.705 13.008 20.221 1.00 15.73                      ATOM 1655 CG HIS A 215 0 20.309 12.543 18.936 1.00 16.90                      ATOM 1656 ND1 HIS A 215 0 19.589 11.864 17.963 1.00 17.35                     ATOM 1657 CD2 HIS A 215 0 21.574 12.658 18.444 1.00 16.15                     ATOM 1658 CE1 HIS A 215 0 20.376 11.576 16.933 1.00 17.63                     ATOM 1659 NE2 HIS A 215 0 21.599 12.046 17.216 1.00 17.73                     ATOM 1660 N GLU A 216 0 20.104 12.815 23.382 1.00 17.22                       ATOM 1661 CA GLU A 216 0 19.876 13.479 24.665 1.00 15.86                      ATOM 1662 C GLU A 216 0 20.070 14.976 24.456 1.00 15.61                       ATOM 1663 O GLU A 216 0 20.684 15.386 23.453 1.00 14.96                       ATOM 1664 CB GLU A 216 0 20.817 12.901 25.694 1.00 15.38                      ATOM 1665 CG GLU A 216 0 20.440 11.520 26.166 1.00 16.53                      ATOM 1666 CD GLU A 216 0 21.242 11.058 27.357 1.00 17.23                      ATOM 1667 OE1 GLU A 216 0 22.378 10.619 27.129 1.00 20.31                     ATOM 1668 OE2 GLU A 216 0 20.813 11.119 28.519 1.00 16.06                     ATOM 1669 N LEU A 217 0 19.623 15.792 25.394 1.00 14.64                       ATOM 1670 CA LEU A 217 0 19.738 17.243 25.251 1.00 14.91                      ATOM 1671 C LEU A 217 0 20.512 17.792 26.446 1.00 14.71                       ATOM 1672 O LEU A 217 0 19.950 17.734 27.539 1.00 15.67                       ATOM 1673 CB LEU A 217 0 18.362 17.931 25.229 1.00 14.75                      ATOM 1674 CG LEU A 217 0 17.276 17.349 24.306 1.00 15.40                      ATOM 1675 CD1 LEU A 217 0 15.939 18.075 24.505 1.00 15.08                     ATOM 1676 CD2 LEU A 217 0 17.723 17.453 22.849 1.00 15.22                     ATOM 1677 N THR A 218 0 21.732 18.278 26.229 1.00 13.65                       ATOM 1678 CA THR A 218 0 22.507 18.714 27.402 1.00 13.26                      ATOM 1679 C THR A 218 0 22.427 20.232 27.505 1.00 13..27                      ATOM 1680 O THR A 218 0 23.142 20.955 26.805 1.00 12.91                       ATOM 1681 CB THR A 218 0 23.955 18.216 27.304 1.00 12.08                      ATOM 1682 OG1 THR A 218 0 23.935 16.782 27.331 1.00 15.48                     ATOM 1683 CG2 THR A 218 0 24.767 18.721 28.470 1.00 11.46                     ATOM 1684 N ILE A 219 0 21.522 20.649 28.385 1.00 13.30                       ATOM 1685 CA ILE A 219 0 21.259 22.068 28.547 1.00 14.53                      ATOM 1686 C ILE A 219 0 22.420 22.818 29.180 1.00 12.72                       ATOM 1687 O ILE A 219 0 22.795 22.492 30.292 1.00 13.08                       ATOM 1688 CB ILE A 219 0 19.930 22.268 29.323 1.00 14.74                      ATOM 1689 CG1 ILE A 219 0 18.761 21.699 28.441 1.00 17.33                     ATOM 1690 CG2 ILE A 219 0 19.666 23.717 29.656 1.00 13.40                     ATOM 1691 CD1 ILE A 219 0 17.597 21.481 29.412 1.00 19.42                     ATOM 1692 N ILE A 220 0 22.898 23.869 28.510 1.00 12.55                       ATOM 1693 CA ILE A 220 0 23.994 24.696 29.019 1.00 13.25                      ATOM 1694 C ILE A 220 0 23.686 26.193 29.085 1.00 15.11                       ATOM 1695 O ILE A 220 0 24.477 27.001 29.618 1.00 14.73                       ATOM 1696 CB ILE A 220 0 25.239 24.507 28.125 1.00 11.80                      ATOM 1697 CG1 ILE A 220 0 24.954 24.871 26.671 1.00 10.93                     ATOM 1698 CG2 ILE A 220 0 25.770 23.072 28.291 1.00 9.59                      ATOM 1699 CD1 ILE A 220 0 26.249 25.231 25.928 1.00 12.07                     ATOM 1700 N GLU A 221 0 22.490 26.573 28.597 1.00 13.30                       ATOM 1701 CA GLU A 221 0 22.048 27.951 28.624 1.00 12.96                      ATOM 1702 C GLU A 221 0 20.522 28.066 28.727 1.00 13.77                       ATOM 1703 O GLU A 221 0 19.799 27.301 28.068 1.00 14.06                       ATOM 1704 CB GLU A 221 0 22.436 28.666 27.318 1.00 12.73                      ATOM 1705 CG GLU A 221 0 22.280 30.178 27.325 1.00 12.94                      ATOM 1706 CD GLU A 221 0 22.018 30.783 25.969 1.00 13.84                      ATOM 1707 OE1 GLU A 221 0 22.345 30.269 24.887 1.00 12.66                     ATOM 1708 OE2 GLU A 221 0 21.386 31.862 25.936 1.00 14.80                     ATOM 1709 N VAL A 222 0 20.062 29.091 29.434 1.00 13.89                       ATOM 1710 CA VAL A 222 0 18.632 29.350 29.534 1.00 14.13                      ATOM 1711 C VAL A 222 0 18.409 30.853 29.493 1.00 13.87                       ATOM 1712 O VAL A 222 0 18.900 31.657 30.300 1.00 11.55                       ATOM 1713 CB VAL A 222 0 18.003 28.649 30.737 1.00 16.86                      ATOM 1714 CG1 VAL A 222 0 18.730 28.941 32.017 1.00 19.16                     ATOM 1715 CG2 VAL A 222 0 16.575 29.120 31.033 1.00 18.45                     ATOM 1716 N ASP A 223 0 17.631 31.267 28.481 1.00 11.69                       ATOM 1717 CA ASP A 223 0 17.245 32.673 28.386 1.00 13.60                      ATOM 1718 C ASP A 223 0 18.472 33.598 28.548 1.00 14.44                       ATOM 1719 O ASP A 223 0 18.423 34.552 29.336 1.00 12.75                       ATOM 1720 CB ASP A 223 0 16.161 33.033 29.417 1.00 12.59                      ATOM 1721 CG ASP A 223 0 14.845 32.279 29.364 1.00 14.64                      ATOM 1722 OD1 ASP A 223 0 14.697 31.397 28.493 1.00 13.34                     ATOM 1723 OD2 ASP A 223 0 13.858 32.463 30.156 1.00 13.85                     ATOM 1724 N GLY A 224 0 19.544 33.372 27.767 1.00 13.49                       ATOM 1725 CA GLY A 224 0 20.728 34.213 27.770 1.00 12.85                      ATOM 1726 C GLY A 224 0 21.562 34.112 29.049 1.00 13.00                       ATOM 1727 O GLY A 224 0 22.326 35.040 29.317 1.00 13.97                       ATOM 1728 N GLU A 225 0 21.370 33.105 29.875 1.00 11.78                       ATOM 1729 CA GLU A 225 0 22.068 32.888 31.114 1.00 14.97                      ATOM 1730 C GLU A 225 0 22.609 31.447 31.106 1.00 16.73                       ATOM 1731 O GLU A 225 0 21.858 30.498 30.849 1.00 15.88                       ATOM 1732 CB GLU A 225 0 21.174 33.062 32.358 1.00 16.54                      ATOM 1733 CG GLU A 225 0 20.509 34.424 32.534 1.00 16.30                      ATOM 1734 CD GLU A 225 0 21.492 35.546 32.823 1.00 17.57                      ATOM 1735 OE1 GLU A 225 0 22.450 35.254 33.561 1.00 18.76                     ATOM 1736 OE2 GLU A 225 0 21.360 36.711 32.360 1.00 17.77                     ATOM 1737 N LEU A 226 0 23.922 31.285 31.324 1.00 16.90                       ATOM 1738 CA LEU A 226 0 24.526 29.955 31.318 1.00 15.50                      ATOM 1739 C LEU A 226 0 24.183 29.127 32.540 1.00 15.04                       ATOM 1740 O LEU A 226 0 24.002 29.648 33.652 1.00 15.17                       ATOM 1741 CB LEU A 226 0 26.062 30.008 31.216 1.00 15.36                      ATOM 1742 CG LEU A 226 0 26.567 30.741 29.958 1.00 17.95                      ATOM 1743 CD1 LEU A 226 0 28.076 30.876 29.979 1.00 18.77                     ATOM 1744 CD2 LEU A 226 0 26.111 30.029 28.687 1.00 17.36                     ATOM 1745 N THR A 227 0 24.119 27.799 32.332 1.00 13.62                       ATOM 1746 CA THR A 227 0 23.848 26.930 33.479 1.00 13.72                      ATOM 1747 C THR A 227 0 24.936 25.851 33.528 1.00 14.30                       ATOM 1748 O THR A 227 0 25.732 25.629 32.592 1.00 14.28                       ATOM 1749 CB THR A 227 0 22.478 26.217 33.352 1.00 14.35                      ATOM 1750 OG1 THR A 227 0 22.506 25.385 32.178 1.00 13.68                     ATOM 1751 CG2 THR A 227 0 21.284 27.161 33.180 1.00 12.29                     ATOM 1752 N GLU A 228 0 24.960 25.136 34.625 1.00 14.73                       ATOM 1753 CA GLU A 228 0 25.765 23.907 34.714 1.00 17.32                      ATOM 1754 C GLU A 228 0 25.110 22.971 33.680 1.00 17.30                       ATOM 1755 O GLU A 228 0 23.917 23.035 33.472 1.00 16.97                       ATOM 1756 CB GLU A 228 0 25.617 23.315 36.114 1.00 16.58                      ATOM 1757 CG GLU A 228 0 26.493 23.979 37.186 1.00 18.10                      ATOM 1758 CD GLU A 228 0 26.236 23.458 38.575 1.00 20.92                      ATOM 1759 OE1 GLU A 228 0 25.469 22.470 38.755 1.00 23.38                     ATOM 1760 OE2 GLU A 228 0 26.769 23.997 39.564 1.00 21.26                     ATOM 1761 N PRO A 229 0 25.867 22.158 32.984 1.00 16.91                       ATOM 1762 CA PRO A 229 0 25.369 21.207 31.992 1.00 16.37                      ATOM 1763 C PRO A 229 0 24.351 20.275 32.599 1.00 16.24                       ATOM 1764 O PRO A 229 0 24.624 19.652 33.619 1.00 15.76                       ATOM 1765 CB PRO A 229 0 26.612 20.469 31.419 1.00 15.97                      ATOM 1766 CG PRO A 229 0 27.701 21.509 31.741 1.00 15.92                      ATOM 1767 CD PRO A 229 0 27.337 22.141 33.083 1.00 14.86                      ATOM 1768 N HIS A 230 0 23.140 20.164 32.038 1.00 15.58                       ATOM 1769 CA HIS A 230 0 22.090 19.325 32.618 1.00 15.01                      ATOM 1770 C HIS A 230 0 21.354 18.610 31.488 1.00 13.55                       ATOM 1771 O HIS A 230 0 20.756 19.192 30.590 1.00 13.47                       ATOM 1772 CB HIS A 230 0 21.172 20.164 33.510 1.00 15.89                      ATOM 1773 CG HIS A 230 0 20.045 19.341 34.064 1.00 18.32                      ATOM 1774 ND1 HIS A 230 0 20.252 18.347 35.004 1.00 18.14                     ATOM 1775 CD2 HIS A 230 0 18.713 19.328 33.791 1.00 17.75                     ATOM 1776 CE1 HIS A 230 0 19.121 17.768 35.310 1.00 16.33                     ATOM 1777 NE2 HIS A 230 0 18.173 18.344 34.609 1.00 17.85                     ATOM 1778 N THR A 231 0 21.496 17.304 31.458 1.00 12.94                       ATOM 1779 CA THR A 231 0 20.995 16.474 30.346 1.00 14.15                      ATOM 1780 C THR A 231 0 19.620 15.890 30.547 1.00 13.41                       ATOM 1781 O THR A 231 0 19.293 15.401 31.616 1.00 14.89                       ATOM 1782 CB THR A 231 0 22.040 15.364 30.060 1.00 13.73                      ATOM 1783 OG1 THR A 231 0 23.314 16.023 29.852 1.00 14.77                     ATOM 1784 CG2 THR A 231 0 21.655 14.600 28.818 1.00 13.06                     ATOM 1785 N VAL A 232 0 18.776 15.954 29.549 1.00 12.86                       ATOM 1786 CA VAL A 232 0 17.374 15.505 29.665 1.00 13.44                      ATOM 1787 C VAL A 232 0 16.999 14.966 28.319 1.00 14.96                       ATOM 1788 O VAL A 232 0 17.790 15.258 27.390 1.00 14.12                       ATOM 1789 CB VAL A 232 0 16.771 16.910 30.000 1.00 17.41                      ATOM 1790 CG1 VAL A 232 0 16.075 17.587 28.856 1.00 14.66                     ATOM 1791 CG2 VAL A 232 0 16.158 16.935 31.371 1.00 15.66                     ATOM 1792 N ASP A 233 0 15.874 14.277 28.153 1.00 14.01                       ATOM 1793 CA ASP A 233 0 15.405 13.803 26.874 1.00 14.73                      ATOM 1794 C ASP A 233 0 14.353 14.718 26.245 1.00 14.74                       ATOM 1795 O ASP A 233 0 14.187 14.731 25.027 1.00 13.41                       ATOM 1796 CB ASP A 233 0 14.640 12.465 27.046 1.00 16.54                      ATOM 1797 CG ASP A 233 0 15.637 11.417 27.536 1.00 19.27                      ATOM 1798 OD1 ASP A 233 0 16.543 11.145 26.732 1.00 20.98                     ATOM 1799 OD2 ASP A 233 0 15.536 10.945 28.667 1.00 19.27                     ATOM 1800 N ARG A 234 0 13.595 15.386 27.122 1.00 13.79                       ATOM 1801 CA ARG A 234 0 12.514 16.199 26.598 1.00 16.36                      ATOM 1802 C ARG A 234 0 12.258 17.426 27.472 1.00 15.17                       ATOM 1803 O ARG A 234 0 12.418 17.390 28.686 1.00 13.96                       ATOM 1804 CB ARG A 234 0 11.265 15.330 26.482 1.00 19.23                      ATOM 1805 CG ARG A 234 0 10.104 16.036 25.788 1.00 22.25                      ATOM 1806 CD ARG A 234 0 8.981 15.023 25.506 1.00 24.68                       ATOM 1807 NE ARG A 234 0 8.157 14.983 26.705 1.00 28.27                       ATOM 1808 CZ ARG A 234 0 6.845 14.828 26.719 1.00 28.66                       ATOM 1809 NH1 ARG A 234 0 6.291 14.833 27.909 1.00 30.08                      ATOM 1810 NH2 ARG A 234 0 6.191 14.662 25.587 1.00 30.24                      ATOM 1811 N LEU A 235 0 11.874 18.524 26.816 1.00 13.90                       ATOM 1812 CA LEU A 235 0 11.619 19.742 27.607 1.00 13.15                      ATOM 1813 C LEU A 235 0 10.390 20.430 27.041 1.00 11.49                       ATOM 1814 O LEU A 235 0 10.025 20.304 25.873 1.00 11.08                       ATOM 1815 CB LEU A 235 0 12.825 20.630 27.695 1.00 14.39                      ATOM 1816 CG LEU A 235 0 13.459 21.645 26.801 1.00 17.19                      ATOM 1817 CD1 LEU A 235 0 14.795 21.218 26.197 1.00 16.98                     ATOM 1818 CD2 LEU A 235 0 12.586 22.219 25.685 1.00 18.24                     ATOM 1819 N GLN A 236 0 9.769 21.152 27.949 1.00 12.74                        ATOM 1820 CA GLN A 236 0 8.576 21.944 27.616 1.00 13.45                       ATOM 1821 C GLN A 236 0 9.005 23.390 27.459 1.00 12.21                        ATOM 1822 O GLN A 236 0 9.606 23.939 28.406 1.00 13.90                        ATOM 1823 CB GLN A 236 0 7.525 21.770 28.741 1.00 12.06                       ATOM 1824 CG GLN A 236 0 6.197 22.276 28.238 1.00 14.12                       ATOM 1825 CD GLN A 236 0 5.025 22.108 29.205 1.00 13.35                       ATOM 1826 OE1 GLN A 236 0 3.893 22.215 28.721 1.00 15.61                      ATOM 1827 NE2 GLN A 236 0 5.226 21.912 30.463 1.00 12.00                      ATOM 1828 N ILE A 237 0 8.748 24.011 26.311 1.00 12.17                        ATOM 1829 CA ILE A 237 0 9.213 25.390 26.156 1.00 12.41                       ATOM 1830 C ILE A 237 0 8.061 26.376 25.953 1.00 13.14                        ATOM 1831 O ILE A 237 0 7.283 26.310 24.990 1.00 13.64                        ATOM 1832 CB ILE A 237 0 10.255 25.437 25.022 1.00 11.03                      ATOM 1833 CG1 ILE A 237 0 10.947 26.793 24.960 1.00 11.84                     ATOM 1834 CG2 ILE A 237 0 9.615 25.086 23.662 1.00 10.02                      ATOM 1835 CD1 ILE A 237 0 12.041 26.953 23.902 1.00 11.23                     ATOM 1836 N PHE A 238 0 8.037 27.414 26.765 1.00 12.83                        ATOM 1837 CA PHE A 238 0 6.979 28.431 26.714 1.00 13.23                       ATOM 1838 C PHE A 238 0 7.382 29.683 25.957 1.00 13.99                        ATOM 1839 O PHE A 238 0 8.530 29.848 25.545 1.00 13.87                        ATOM 1840 CB PHE A 238 0 6.592 28.848 28.145 1.00 12.72                       ATOM 1841 CG PHE A 238 0 6.176 27.691 28.993 1.00 14.51                       ATOM 1842 CD1 PHE A 238 0 7.098 26.957 29.710 1.00 14.84                      ATOM 1843 CD2 PHE A 238 0 4.836 27.314 29.078 1.00 15.50                      ATOM 1844 CE1 PHE A 238 0 6.748 25.882 30.497 1.00 13.87                      ATOM 1845 CE2 PHE A 238 0 4.468 26.236 29.862 1.00 14.62                      ATOM 1846 CZ PHE A 238 0 5.423 25.528 30.568 1.00 15.15                       ATOM 1847 N THR A 239 0 6.388 30.494 25.604 1.00 14.16                        ATOM 1848 CA THR A 239 0 6.543 31.678 24.806 1.00 13.44                       ATOM 1849 C THR A 239 0 7.832 32.453 25.106 1.00 11.74                        ATOM 1850 O THR A 239 0 8.012 32.950 26.218 1.00 10.47                        ATOM 1851 CB THR A 239 0 5.381 32.695 24.978 1.00 15.55                       ATOM 1852 OG1 THR A 239 0 5.258 33.008 26.359 1.00 17.88                      ATOM 1853 CG2 THR A 239 0 4.055 32.131 24.478 1.00 16.75                      ATOM 1854 N GLY A 240 0 8.672 32.593 24.078 1.00 7.94                         ATOM 1855 CA GLY A 240 0 9.877 33.348 24.193 1.00 10.08                       ATOM 1856 C GLY A 240 0 11.039 32.865 25.041 1.00 11.34                       ATOM 1857 O GLY A 240 0 11.977 33.650 25.216 1.00 11.02                       ATOM 1858 N GLN A 241 0 10.990 31.646 25.592 1.00 9.73                        ATOM 1859 CA GLN A 241 0 12.067 31.090 26.364 1.00 9.59                       ATOM 1860 C GLN A 241 0 13.114 30.587 25.342 1.00 10.56                       ATOM 1861 O GLN A 241 0 12.823 30.467 24.126 1.00 8.44                        ATOM 1862 CB GLN A 241 0 11.604 29.965 27.285 1.00 10.57                      ATOM 1863 CG GLN A 241 0 10.820 30.363 28.523 1.00 10.54                      ATOM 1864 CD GLN A 241 0 10.341 29.190 29.341 1.00 12.22                      ATOM 1865 OE1 GLN A 241 0 10.118 28.077 28.815 1.00 13.21                     ATOM 1866 NE2 GLN A 241 0 10.220 29.466 30.639 1.00 11.74                     ATOM 1867 N ARG A 242 0 14.372 30.492 25.774 1.00 9.00                        ATOM 1868 CA ARG A 242 0 15.388 29.992 24.834 1.00 11.01                      ATOM 1869 C ARG A 242 0 16.210 28.966 25.609 1.00 11.30                       ATOM 1870 O ARG A 242 0 16.292 29.133 26.816 1.00 9.51                        ATOM 1871 CB ARG A 242 0 16.324 31.043 24.265 1.00 12.77                      ATOM 1872 CG ARG A 242 0 15.694 32.128 23.364 1.00 12.52                      ATOM 1873 CD ARG A 242 0 15.066 33.249 24.138 1.00 10.81                      ATOM 1874 NE ARG A 242 0 15.957 34.126 24.892 1.00 10.80                      ATOM 1875 CZ ARG A 242 0 15.630 34.761 26.002 1.00 11.36                      ATOM 1876 NH1 ARG A 242 0 16.486 35.548 26.648 1.00 7.98                      ATOM 1877 NH2 ARG A 242 0 14.365 34.589 26.489 1.00 12.78                     ATOM 1878 N TYR A 243 0 16.717 27.934 24.942 1.00 11.61                       ATOM 1879 CA TYR A 243 0 17.631 27.009 25.610 1.00 12.54                      ATOM 1880 C TYR A 243 0 18.819 26.762 24.650 1.00 14.46                       ATOM 1881 O TYR A 243 0 18.568 26.656 23.435 1.00 16.11                       ATOM 1882 CB TYR A 243 0 17.015 25.638 25.934 1.00 11.09                      ATOM 1883 CG TYR A 243 0 16.007 25.667 27.054 1.00 12.11                      ATOM 1884 CD1 TYR A 243 0 14.641 25.825 26.843 1.00 12.88                     ATOM 1885 CD2 TYR A 243 0 16.440 25.575 28.371 1.00 12.11                     ATOM 1886 CE1 TYR A 243 0 13.748 25.869 27.915 1.00 12.71                     ATOM 1887 CE2 TYR A 243 0 15.560 25.582 29.436 1.00 12.50                     ATOM 1888 CZ TYR A 243 0 14.205 25.738 29.188 1.00 12.29                      ATOM 1889 OH TYR A 243 0 13.379 25.789 30.286 1.00 13.65                      ATOM 1890 N SER A 244 0 20.059 26.734 25.144 1.00 12.78                       ATOM 1891 CA SER A 244 0 21.117 26.212 24.268 1.00 13.22                      ATOM 1892 C SER A 244 0 21.333 24.779 24.814 1.00 11.06                       ATOM 1893 O SER A 244 0 21.377 24.604 26.018 1.00 11.27                       ATOM 1894 CB SER A 244 0 22.485 26.907 24.308 1.00 14.46                      ATOM 1895 OG SER A 244 0 22.551 28.029 23.463 1.00 13.59                      ATOM 1896 N PHE A 245 0 21.484 23.780 23.983 1.00 11.89                       ATOM 1897 CA PHE A 245 0 21.772 22.437 24.452 1.00 13.14                      ATOM 1898 C PHE A 245 0 22.867 21.857 23.546 1.00 12.32                       ATOM 1899 O PHE A 245 0 22.890 22.128 22.354 1.00 11.11                       ATOM 1900 CB PHE A 245 0 20.554 21.495 24.526 1.00 11.40                      ATOM 1901 CG PHE A 245 0 19.915 21.236 23.195 1.00 11.98                      ATOM 1902 CD1 PHE A 245 0 18.815 21.993 22.813 1.00 13.38                     ATOM 1903 CD2 PHE A 245 0 20.349 20.236 22.351 1.00 11.45                     ATOM 1904 CE1 PHE A 245 0 18.216 21.773 21.588 1.00 12.84                     ATOM 1905 CE2 PHE A 245 0 19.759 20.000 21.129 1.00 11.48                     ATOM 1906 CZ PHE A 245 0 18.705 20.796 20.743 1.00 12.65                      ATOM 1907 N VAL A 246 0 23.742 21.073 24.169 1.00 13.51                       ATOM 1908 CA VAL A 246 0 24.775 20.427 23.341 1.00 13.37                      ATOM 1909 C VAL A 246 0 24.096 19.177 22.783 1.00 12.47                       ATOM 1910 O VAL A 246 0 23.505 18.425 23.540 1.00 11.41                       ATOM 1911 CB VAL A 246 0 25.990 19.984 24.190 1.00 14.96                      ATOM 1912 CG1 VAL A 246 0 26.995 19.186 23.364 1.00 13.75                     ATOM 1913 CG2 VAL A 246 0 26.681 21.165 24.841 1.00 15.92                     ATOM 1914 N LEU A 247 0 24.160 18.996 21.490 1.00 12.97                       ATOM 1915 CA LEU A 247 0 23.766 17.833 20.785 1.00 14.32                      ATOM 1916 C LEU A 247 0 25.071 17.077 20.395 1.00 14.22                       ATOM 1917 O LEU A 247 0 25.954 17.529 19.664 1.00 12.45                       ATOM 1918 CB LEU A 247 0 22.980 18.109 19.505 1.00 16.00                      ATOM 1919 CG LEU A 247 0 22.514 16.786 18.835 1.00 16.80                      ATOM 1920 CD1 LEU A 247 0 21.266 16.306 19.513 1.00 18.30                     ATOM 1921 CD2 LEU A 247 0 22.207 16.988 17.373 1.00 18.70                     ATOM 1922 N ASP A 248 0 25.144 15.886 20.926 1.00 13.56                       ATOM 1923 CA ASP A 248 0 26.278 14.980 20.727 1.00 16.65                      ATOM 1924 C ASP A 248 0 25.916 14.072 19.581 1.00 16.18                       ATOM 1925 O ASP A 248 0 25.095 13.166 19.813 1.00 17.60                       ATOM 1926 CB ASP A 248 0 26.536 14.229 22.036 1.00 17.83                      ATOM 1927 CG ASP A 248 0 27.798 13.359 22.024 1.00 21.77                      ATOM 1928 OD1 ASP A 248 0 28.231 12.967 23.140 1.00 24.11                     ATOM 1929 OD2 ASP A 248 0 28.345 13.060 20.950 1.00 21.25                     ATOM 1930 N ALA A 249 0 26.414 14.277 18.369 1.00 15.85                       ATOM 1931 CA ALA A 249 0 25.982 13.416 17.255 1.00 17.99                      ATOM 1932 C ALA A 249 0 26.698 12.049 17.306 1.00 20.21                       ATOM 1933 O ALA A 249 0 27.569 11.766 16.485 1.00 19.11                       ATOM 1934 CB ALA A 249 0 26.165 14.126 15.930 1.00 14.57                      ATOM 1935 N ASN A 250 0 26.273 11.223 18.253 1.00 21.66                       ATOM 1936 CA ASN A 250 0 26.861 9.961 18.581 1.00 25.53                       ATOM 1937 C ASN A 250 0 26.061 8.721 18.202 1.00 27.30                        ATOM 1938 O ASN A 250 0 26.344 7.645 18.756 1.00 29.42                        ATOM 1939 CB ASN A 250 0 27.108 9.912 20.104 1.00 25.83                       ATOM 1940 CG ASN A 250 0 25.888 9.968 20.978 1.00 28.76                       ATOM 1941 OD1 ASN A 250 0 24.757 10.156 20.527 1.00 29.90                     ATOM 1942 ND2 ASN A 250 0 26.042 9.826 22.306 1.00 29.52                      ATOM 1943 N GLN A 251 0 25.089 8.841 17.302 1.00 26.74                        ATOM 1944 CA GLN A 251 0 24.239 7.712 16.934 1.00 23.48                       ATOM 1945 C GLN A 251 0 24.583 7.311 15.510 1.00 21.73                        ATOM 1946 O GLN A 251 0 25.333 8.009 14.843 1.00 19.39                        ATOM 1947 CB GLN A 251 0 22.757 8.104 17.022 1.00 24.79                       ATOM 1948 CG GLN A 251 0 22.333 8.701 18.360 1.00 25.14                       ATOM 1949 CD GLN A 251 0 22.430 7.693 19.480 1.00 26.76                       ATOM 1950 OE1 GLN A 251 0 21.762 6.654 19.405 1.00 28.78                      ATOM 1951 NE2 GLN A 251 0 23.202 7.986 20.514 1.00 26.02                      ATOM 1952 N PRO A 252 0 24.058 6.177 15.076 1.00 20.53                        ATOM 1953 CA PRO A 252 0 24.293 5.637 13.755 1.00 20.06                       ATOM 1954 C PRO A 252 0 23.940 6.671 12.702 1.00 21.83                        ATOM 1955 O PRO A 252 0 22.973 7.424 12.940 1.00 22.51                        ATOM 1956 CB PRO A 252 0 23.417 4.367 13.647 1.00 19.98                       ATOM 1957 CG PRO A 252 0 23.288 3.997 15.096 1.00 19.94                       ATOM 1958 CD PRO A 252 0 23.223 5.289 15.902 1.00 19.68                       ATOM 1959 N VAL A 253 0 24.663 6.728 11.584 1.00 20.85                        ATOM 1960 CA VAL A 253 0 24.302 7.741 10.604 1.00 22.29                       ATOM 1961 C VAL A 253 0 22.897 7.414 10.108 1.00 23.02                        ATOM 1962 O VAL A 253 0 22.593 6.289 9.753 1.00 21.37                         ATOM 1963 CB VAL A 253 0 25.298 8.065 9.494 1.00 23.22                        ATOM 1964 CG1 VAL A 253 0 26.696 7.582 9.827 1.00 22.25                       ATOM 1965 CG2 VAL A 253 0 24.859 7.680 8.101 1.00 22.26                       ATOM 1966 N ASP A 254 0 22.012 8.422 10.159 1.00 24.32                        ATOM 1967 CA ASP A 254 0 20.613 8.176 9.786 1.00 22.09                        ATOM 1968 C ASP A 254 0 19.782 9.448 9.821 1.00 20.71                         ATOM 1969 O ASP A 254 0 20.365 10.481 10.099 1.00 18.92                       ATOM 1970 CB ASP A 254 0 20.048 7.211 10.830 1.00 23.39                       ATOM 1971 CG ASP A 254 0 18.964 6.331 10.251 1.00 24.43                       ATOM 1972 OD1 ASP A 254 0 18.355 6.663 9.239 1.00 23.21                       ATOM 1973 OD2 ASP A 254 0 18.736 5.244 10.816 1.00 28.26                      ATOM 1974 N ASN A 255 0 18.485 9.338 9.496 1.00 18.97                         ATOM 1975 CA ASN A 255 0 17.583 10.479 9.599 1.00 17.69                       ATOM 1976 C ASN A 255 0 16.785 10.335 10.889 1.00 17.64                       ATOM 1977 O ASN A 255 0 16.390 9.204 11.249 1.00 17.75                        ATOM 1978 CB ASN A 255 0 16.663 10.554 8.386 1.00 17.19                       ATOM 1979 CG ASN A 255 0 17.467 10.882 7.143 1.00 17.33                       ATOM 1980 OD1 ASN A 255 0 17.891 12.023 6.932 1.00 18.05                      ATOM 1981 ND2 ASN A 255 0 17.649 9.913 6.263 1.00 15.98                       ATOM 1982 N TYR A 256 0 16.657 11.403 11.684 1.00 14.89                       ATOM 1983 CA TYR A 256 0 15.983 11.364 12.961 1.00 12.56                      ATOM 1984 C TYR A 256 0 14.966 12.520 12.991 1.00 15.02                       ATOM 1985 O TYR A 256 0 15.208 13.637 12.509 1.00 14.49                       ATOM 1986 CB TYR A 256 0 16.867 11.479 14.216 1.00 14.85                      ATOM 1987 CG TYR A 256 0 17.883 10.349 14.316 1.00 13.96                      ATOM 1988 CD1 TYR A 256 0 19.030 10.427 13.529 1.00 13.97                     ATOM 1989 CD2 TYR A 256 0 17.712 9.245 15.129 1.00 14.62                      ATOM 1990 CE1 TYR A 256 0 19.986 9.422 13.534 1.00 13.83                      ATOM 1991 CE2 TYR A 256 0 18.667 8.224 15.170 1.00 15.31                      ATOM 1992 CZ TYR A 256 0 19.795 8.336 14.346 1.00 15.90                       ATOM 1993 OH TYR A 256 0 20.763 7.341 14.337 1.00 17.15                       ATOM 1994 N TRP A 257 0 13.801 12.198 13.564 1.00 13.58                       ATOM 1995 CA TRP A 257 0 12.742 13.196 13.657 1.00 14.21                      ATOM 1996 C TRP A 257 0 13.041 14.198 14.769 1.00 12.04                       ATOM 1997 O TRP A 257 0 13.382 13.811 15.878 1.00 10.46                       ATOM 1998 CB TRP A 257 0 11.363 12.592 13.988 1.00 12.49                      ATOM 1999 CG TRP A 257 0 10.648 11.906 12.865 1.00 13.06                      ATOM 2000 CD1 TRP A 257 0 10.315 10.568 12.879 1.00 12.86                     ATOM 2001 CD2 TRP A 257 0 10.161 12.437 11.633 1.00 12.33                     ATOM 2002 NE1 TRP A 257 0 9.640 10.267 11.720 1.00 13.75                      ATOM 2003 CE2 TRP A 257 0 9.530 11.388 10.940 1.00 13.78                      ATOM 2004 CE3 TRP A 257 0 10.173 13.691 11.035 1.00 14.13                     ATOM 2005 CZ2 TRP A 257 0 8.940 11.538 9.681 1.00 13.24                       ATOM 2006 CZ3 TRP A 257 0 9.590 13.868 9.786 1.00 14.34                       ATOM 2007 CH2 TRP A 257 0 8.963 12.789 9.127 1.00 13.64                       ATOM 2008 N ILE A 258 0 12.790 15.463 14.454 1.00 12.29                       ATOM 2009 CA ILE A 258 0 12.886 16.498 15.508 1.00 12.44                      ATOM 2010 C ILE A 258 0 11.391 16.840 15.769 1.00 12.40                       ATOM 2011 O ILE A 258 0 10.629 17.039 14.812 1.00 12.43                       ATOM 2012 CB ILE A 258 0 13.617 17.777 15.048 1.00 13.32                      ATOM 2013 CG1 ILE A 258 0 15.107 17.477 14.854 1.00 14.52                     ATOM 2014 CG2 ILE A 258 0 13.365 18.888 16.052 1.00 12.32                     ATOM 2015 CD1 ILE A 258 0 15.839 18.474 13.994 1.00 14.35                     ATOM 2016 N ARG A 259 0 11.017 16.764 17.013 1.00 11.51                       ATOM 2017 CA ARG A 259 0 9.610 16.832 17.407 1.00 13.43                       ATOM 2018 C ARG A 259 0 9.254 18.019 18.274 1.00 12.74                        ATOM 2019 O ARG A 259 0 9.931 18.246 19.280 1.00 12.62                        ATOM 2020 CB ARG A 259 0 9.326 15.567 18.253 1.00 12.43                       ATOM 2021 CG ARG A 259 0 9.308 14.290 17.414 1.00 15.81                       ATOM 2022 CD ARG A 259 0 8.910 13.054 18.244 1.00 16.58                       ATOM 2023 NE ARG A 259 0 9.204 11.818 17.528 1.00 16.91                       ATOM 2024 CZ ARG A 259 0 8.475 11.187 16.616 1.00 18.43                       ATOM 2025 NH1 ARG A 259 0 7.285 11.657 16.239 1.00 19.39                      ATOM 2026 NH2 ARG A 259 0 8.907 10.070 16.045 1.00 17.95                      ATOM 2027 N ALA A 260 0 8.226 18.764 17.884 1.00 13.12                        ATOM 2028 CA ALA A 260 0 7.768 19.882 18.727 1.00 12.65                       ATOM 2029 C ALA A 260 0 6.237 19.763 18.802 1.00 14.47                        ATOM 2030 O ALA A 260 0 5.545 20.140 17.868 1.00 14.73                        ATOM 2031 CB ALA A 260 0 8.281 21.188 18.165 1.00 9.58                        ATOM 2032 N GLN A 261 0 5.690 19.225 19.870 1.00 14.78                        ATOM 2033 CA GLN A 261 0 4.272 19.004 20.060 1.00 16.99                       ATOM 2034 C GLN A 261 0 3.606 20.154 20.803 1.00 15.01                        ATOM 2035 O GLN A 261 0 3.914 20.389 21.961 1.00 13.86                        ATOM 2036 CB GLN A 261 0 4.118 17.747 20.924 1.00 20.94                       ATOM 2037 CG GLN A 261 0 2.717 17.131 20.940 1.00 27.53                       ATOM 2038 CD GLN A 261 0 2.721 15.991 21.947 1.00 29.63                       ATOM 2039 OE1 GLN A 261 0 3.152 14.887 21.682 1.00 31.60                      ATOM 2040 NE2 GLN A 261 0 2.331 16.255 23.188 1.00 34.91                      ATOM 2041 N PRO A 262 0 2.663 20.820 20.167 1.00 14.60                        ATOM 2042 CA PRO A 262 0 1.974 21.969 20.739 1.00 15.72                       ATOM 2043 C PRO A 262 0 0.921 21.568 21.757 1.00 16.25                        ATOM 2044 O PRO A 262 0 0.498 20.409 21.814 1.00 15.61                        ATOM 2045 CB PRO A 262 0 1.401 22.752 19.539 1.00 13.88                       ATOM 2046 CG PRO A 262 0 1.168 21.608 18.563 1.00 13.62                       ATOM 2047 CD PRO A 262 0 2.257 20.570 18.772 1.00 13.23                       ATOM 2048 N ASN A 263 0 0.570 22.481 22.665 1.00 17.25                        ATOM 2049 CA ASN A 263 0 -0.471 22.203 23.648 1.00 17.50                      ATOM 2050 C ASN A 263 0 -1.834 22.460 22.981 1.00 18.43                       ATOM 2051 O ASN A 263 0 -2.810 22.121 23.608 1.00 19.35                       ATOM 2052 CB ASN A 263 0 -0.422 22.990 24.954 1.00 16.12                      ATOM 2053 CG ASN A 263 0 -0.333 24.493 24.728 1.00 16.97                      ATOM 2054 OD1 ASN A 263 0 0.236 25.002 23.751 1.00 15.54                      ATOM 2055 ND2 ASN A 263 0 -0.905 25.269 25.653 1.00 16.31                     ATOM 2056 N LYS A 264 0 -1.947 23.055 21.818 1.00 20.51                       ATOM 2057 CA LYS A 264 0 -3.256 23.208 21.180 1.00 24.76                      ATOM 2058 C LYS A 264 0 -3.055 23.395 19.683 1.00 23.64                       ATOM 2059 O LYS A 264 0 -1.909 23.572 19.267 1.00 24.23                       ATOM 2060 CB LYS A 264 0 -4.038 24.393 21.775 1.00 25.87                      ATOM 2061 CG LYS A 264 0 -3.266 25.702 21.602 1.00 28.62                      ATOM 2062 CD LYS A 264 0 -3.579 26.624 22.772 1.00 30.65                      ATOM 2063 CE LYS A 264 0 -4.114 27.960 22.283 1.00 32.62                      ATOM 2064 NZ LYS A 264 0 -4.593 28.753 23.459 1.00 34.39                      ATOM 2065 N GLY A 265 0 -4.112 23.386 18.892 1.00 22.60                       ATOM 2066 CA GLY A 265 0 -3.959 23.591 17.452 1.00 22.98                      ATOM 2067 C GLY A 265 0 -5.190 23.002 16.758 1.00 23.95                       ATOM 2068 O GLY A 265 0 -5.904 22.202 17.362 1.00 22.64                       ATOM 2069 N ARG A 266 0 -5.398 23.434 15.537 1.00 24.60                       ATOM 2070 CA ARG A 266 0 -6.527 23.051 14.734 1.00 26.24                      ATOM 2071 C ARG A 266 0 -6.412 21.605 14.272 1.00 27.29                       ATOM 2072 O ARG A 266 0 -5.329 21.074 14.015 1.00 25.41                       ATOM 2073 CB ARG A 266 0 -6.628 23.903 13.469 1.00 30.71                      ATOM 2074 CG ARG A 266 0 -7.065 25.334 13.563 1.00 35.66                      ATOM 2075 CD ARG A 266 0 -8.161 25.673 12.539 1.00 40.48                      ATOM 2076 NE ARG A 266 0 -9.379 25.957 13.286 1.00 45.08                      ATOM 2077 CZ ARG A 266 0 -10.551 25.334 13.319 1.00 47.09                     ATOM 2078 NH1 ARG A 266 0 -10.921 24.294 12.577 1.00 48.10                    ATOM 2079 NH2 ARG A 266 0 -11.452 25.828 14.165 1.00 47.80                    ATOM 2080 N ASN A 267 0 -7.586 20.983 14.141 1.00 25.17                       ATOM 2081 CA ASN A 267 0 -7.727 19.669 13.602 1.00 23.96                      ATOM 2082 C ASN A 267 0 -6.859 18.625 14.244 1.00 22.35                       ATOM 2083 O ASN A 267 0 -6.306 17.864 13.448 1.00 23.57                       ATOM 2084 CB ASN A 267 0 -7.390 19.695 12.098 1.00 26.46                      ATOM 2085 CG ASN A 267 0 -8.461 20.426 11.309 1.00 29.21                      ATOM 2086 OD1 ASN A 267 0 -8.190 21.226 10.405 1.00 30.18                     ATOM 2087 ND2 ASN A 267 0 -9.681 20.075 11.701 1.00 28.77                     ATOM 2088 N GLY A 268 0 -6.706 18.594 15.550 1.00 21.85                       ATOM 2089 CA GLY A 268 0 -5.890 17.533 16.121 1.00 22.47                      ATOM 2090 C GLY A 268 0 -4.383 17.760 16.118 1.00 23.29                       ATOM 2091 O GLY A 268 0 -3.652 16.898 16.632 1.00 23.28                       ATOM 2092 N LEU A 269 0 -3.880 18.901 15.676 1.00 22.69                       ATOM 2093 CA LEU A 269 0 -2.454 19.222 15.684 1.00 22.62                      ATOM 2094 C LEU A 269 0 -1.753 18.890 16.990 1.00 23.26                       ATOM 2095 O LEU A 269 0 -0.650 18.335 17.035 1.00 23.42                       ATOM 2096 CB LEU A 269 0 -2.311 20.713 15.472 1.00 22.28                      ATOM 2097 CG LEU A 269 0 -1.183 21.414 14.745 1.00 23.42                      ATOM 2098 CD1 LEU A 269 0 -0.508 22.380 15.682 1.00 19.64                     ATOM 2099 CD2 LEU A 269 0 -0.213 20.492 14.009 1.00 21.26                     ATOM 2100 N ALA A 270 0 -2.371 19.199 18.135 1.00 21.51                       ATOM 2101 CA ALA A 270 0 -1.784 18.899 19.419 1.00 22.26                      ATOM 2102 C ALA A 270 0 -1.612 17.415 19.680 1.00 23.22                       ATOM 2103 O ALA A 270 0 -0.898 17.077 20.637 1.00 21.81                       ATOM 2104 CB ALA A 270 0 -2.632 19.518 20.542 1.00 21.06                      ATOM 2105 N GLY A 271 0 -2.337 16.521 18.996 1.00 23.75                       ATOM 2106 CA GLY A 271 0 -2.190 15.125 19.372 1.00 24.98                      ATOM 2107 C GLY A 271 0 -1.507 14.267 18.328 1.00 26.07                       ATOM 2108 O GLY A 271 0 -1.501 13.045 18.523 1.00 26.26                       ATOM 2109 N THR A 272 0 -0.906 14.825 17.278 1.00 26.48                       ATOM 2110 CA THR A 272 0 -0.327 13.901 16.294 1.00 25.27                      ATOM 2111 C THR A 272 0 0.986 14.362 15.701 1.00 25.58                        ATOM 2112 O THR A 272 0 1.216 15.567 15.701 1.00 24.46                        ATOM 2113 CB THR A 272 0 -1.380 13.759 15.164 1.00 24.40                      ATOM 2114 OG1 THR A 272 0 -0.931 12.737 14.275 1.00 26.32                     ATOM 2115 CG2 THR A 272 0 -1.575 15.022 14.347 1.00 22.50                     ATOM 2116 N PHE A 273 0 1.714 13.443 15.062 1.00 24.01                        ATOM 2117 CA PHE A 273 0 2.897 13.755 14.271 1.00 23.99                       ATOM 2118 C PHE A 273 0 2.663 13.201 12.858 1.00 24.84                        ATOM 2119 O PHE A 273 0 3.534 13.207 11.987 1.00 24.73                        ATOM 2120 CB PHE A 273 0 4.175 13.094 14.812 1.00 22.16                       ATOM 2121 CG PHE A 273 0 4.550 13.676 16.153 1.00 21.84                       ATOM 2122 CD1 PHE A 273 0 4.190 13.037 17.327 1.00 20.67                      ATOM 2123 CD2 PHE A 273 0 5.221 14.881 16.216 1.00 20.98                      ATOM 2124 CE1 PHE A 273 0 4.538 13.574 18.554 1.00 21.75                      ATOM 2125 CE2 PHE A 273 0 5.559 15.428 17.440 1.00 21.65                      ATOM 2126 CZ PHE A 273 0 5.216 14.787 18.616 1.00 22.38                       ATOM 2127 N ALA A 274 0 1.440 12.718 12.647 1.00 24.38                        ATOM 2128 CA ALA A 274 0 1.094 12.053 11.397 1.00 24.29                       ATOM 2129 C ALA A 274 0 1.399 12.920 10.194 1.00 24.15                        ATOM 2130 O ALA A 274 0 0.990 14.078 10.161 1.00 23.07                        ATOM 2131 CB ALA A 274 0 -0.385 11.681 11.387 1.00 23.53                      ATOM 2132 N ASN A 275 0 2.075 12.355 9.204 1.00 23.41                         ATOM 2133 CA ASN A 275 0 2.389 13.068 7.987 1.00 24.88                        ATOM 2134 C ASN A 275 0 3.498 14.093 8.191 1.00 22.73                         ATOM 2135 O ASN A 275 0 3.708 14.947 7.337 1.00 21.57                         ATOM 2136 CB ASN A 275 0 1.138 13.806 7.516 1.00 30.04                        ATOM 2137 CG ASN A 275 0 0.194 13.070 6.633 1.00 35.28                        ATOM 2138 OD1 ASN A 275 0 -0.458 12.071 6.985 1.00 36.92                      ATOM 2139 ND2 ASN A 275 0 0.156 13.655 5.427 1.00 37.87                       ATOM 2140 N GLY A 276 0 4.185 14.083 9.322 1.00 22.10                         ATOM 2141 CA GLY A 276 0 5.278 15.025 9.503 1.00 20.95                        ATOM 2142 C GLY A 276 0 4.801 16.392 9.962 1.00 19.61                         ATOM 2143 O GLY A 276 0 5.587 17.325 9.816 1.00 19.96                         ATOM 2144 N VAL A 277 0 3.600 16.504 10.540 1.00 16.82                        ATOM 2145 CA VAL A 277 0 3.207 17.796 11.107 1.00 15.06                       ATOM 2146 C VAL A 277 0 4.033 17.942 12.379 1.00 13.80                        ATOM 2147 O VAL A 277 0 4.454 16.912 12.926 1.00 13.80                        ATOM 2148 CB VAL A 277 0 1.676 17.849 11.397 1.00 14.37                       ATOM 2149 CG1 VAL A 277 0 0.882 17.824 10.099 1.00 13.37                      ATOM 2150 CG2 VAL A 277 0 1.213 16.763 12.330 1.00 11.77                      ATOM 2151 N ASN A 278 0 4.307 19.100 12.936 1.00 14.25                        ATOM 2152 CA ASN A 278 0 5.026 19.262 14.209 1.00 13.80                       ATOM 2153 C ASN A 278 0 6.443 18.640 14.208 1.00 13.80                        ATOM 2154 O ASN A 278 0 7.020 18.228 15.229 1.00 11.81                        ATOM 2155 CB ASN A 278 0 4.216 18.607 15.312 1.00 14.24                       ATOM 2156 CG ASN A 278 0 2.890 19.288 15.659 1.00 15.35                       ATOM 2157 OD1 ASN A 278 0 1.952 18.531 16.009 1.00 14.81                      ATOM 2158 ND2 ASN A 278 0 2.821 20.591 15.593 1.00 10.69                      ATOM 2159 N SER A 279 0 7.044 18.595 13.025 1.00 12.68                        ATOM 2160 CA SER A 279 0 8.296 17.892 12.860 1.00 15.48                       ATOM 2161 C SER A 279 0 9.323 18.571 11.964 1.00 15.07                        ATOM 2162 O SER A 279 0 8.995 19.309 11.044 1.00 12.20                        ATOM 2163 CB SER A 279 0 7.976 16.549 12.122 1.00 14.76                       ATOM 2164 CG SER A 279 0 7.268 15.722 13.054 1.00 19.57                       ATOM 2165 N ALA A 280 0 10.570 18.152 12.229 1.00 15.67                       ATOM 2166 CA ALA A 280 0 11.664 18.548 11.327 1.00 16.75                      ATOM 2167 C ALA A 280 0 12.620 17.341 11.287 1.00 15.83                       ATOM 2168 O ALA A 280 0 12.438 16.346 11.997 1.00 15.55                       ATOM 2169 CB ALA A 280 0 12.363 19.828 11.745 1.00 16.40                      ATOM 2170 N ILE A 281 0 13.669 17.478 10.485 1.00 14.79                       ATOM 2171 CA ILE A 281 0 14.569 16.346 10.257 1.00 15.55                      ATOM 2172 C ILE A 281 0 16.002 16.610 10.699 1.00 15.92                       ATOM 2173 O ILE A 281 0 16.649 17.577 10.284 1.00 14.96                       ATOM 2174 CB ILE A 281 0 14.557 16.013 8.735 1.00 16.44                       ATOM 2175 CG1 ILE A 281 0 13.147 15.573 8.275 1.00 16.42                      ATOM 2176 CG2 ILE A 281 0 15.615 14.959 8.421 1.00 15.71                      ATOM 2177 CD1 ILE A 281 0 12.981 15.376 6.771 1.00 14.22                      ATOM 2178 N LEU A 282 0 16.505 15.698 11.515 1.00 16.76                       ATOM 2179 CA LEU A 282 0 17.920 15.736 11.912 1.00 15.82                      ATOM 2180 C LEU A 282 0 18.655 14.747 10.990 1.00 16.16                       ATOM 2181 O LEU A 282 0 18.409 13.530 11.034 1.00 16.41                       ATOM 2182 CB LEU A 282 0 18.129 15.400 13.379 1.00 14.54                      ATOM 2183 CG LEU A 282 0 19.632 15.346 13.773 1.00 16.00                      ATOM 2184 CD1 LEU A 282 0 20.100 16.767 14.052 1.00 16.10                     ATOM 2185 CD2 LEU A 282 0 19.865 14.469 14.970 1.00 13.21                     ATOM 2186 N ARG A 283 0 19.490 15.254 10.100 1.00 15.20                       ATOM 2187 CA ARG A 283 0 20.160 14.377 9.141 1.00 16.98                       ATOM 2188 C ARG A 283 0 21.683 14.326 9.279 1.00 17.31                        ATOM 2189 O ARG A 283 0 22.398 15.330 9.203 1.00 17.82                        ATOM 2190 CB ARG A 283 0 19.844 14.861 7.736 1.00 17.30                       ATOM 2191 CG ARG A 283 0 20.417 13.978 6.641 1.00 19.94                       ATOM 2192 CD ARG A 283 0 19.860 14.446 5.301 1.00 20.04                       ATOM 2193 NE ARG A 283 0 18.474 14.010 5.208 1.00 21.56                       ATOM 2194 CZ ARG A 283 0 17.479 14.530 4.505 1.00 21.81                       ATOM 2195 NH1 ARG A 283 0 16.287 13.922 4.564 1.00 21.52                      ATOM 2196 NH2 ARG A 283 0 17.653 15.634 3.797 1.00 21.84                      ATOM 2197 N TYR A 284 0 22.163 13.136 9.567 1.00 16.79                        ATOM 2198 CA TYR A 284 0 23.581 12.821 9.620 1.00 16.35                       ATOM 2199 C TYR A 284 0 24.155 12.787 8.198 1.00 16.52                        ATOM 2200 O TYR A 284 0 23.556 12.226 7.271 1.00 16.33                        ATOM 2201 CB TYR A 284 0 23.730 11.444 10.252 1.00 16.51                      ATOM 2202 CG TYR A 284 0 23.727 11.460 11.755 1.00 17.09                      ATOM 2203 CD1 TYR A 284 0 24.910 11.178 12.437 1.00 17.37                     ATOM 2204 CD2 TYR A 284 0 22.601 11.753 12.504 1.00 17.15                     ATOM 2205 CE1 TYR A 284 0 24.937 11.163 13.817 1.00 17.64                     ATOM 2206 CE2 TYR A 284 0 22.623 11.770 13.892 1.00 15.66                     ATOM 2207 CZ TYR A 284 0 23.796 11.476 14.542 1.00 15.99                      ATOM 2208 OH TYR A 284 0 23.873 11.448 15.919 1.00 14.03                      ATOM 2209 N ALA A 285 0 25.276 13.463 7.992 1.00 17.42                        ATOM 2210 CA ALA A 285 0 25.950 13.461 6.692 1.00 19.35                       ATOM 2211 C ALA A 285 0 26.186 11.994 6.328 1.00 19.20                        ATOM 2212 O ALA A 285 0 26.692 11.237 7.146 1.00 17.18                        ATOM 2213 CB ALA A 285 0 27.293 14.194 6.770 1.00 19.86                       ATOM 2214 N GLY A 286 0 25.724 11.614 5.153 1.00 20.01                        ATOM 2215 CA GLY A 286 0 25.851 10.224 4.747 1.00 21.88                       ATOM 2216 C GLY A 286 0 24.507 9.510 4.754 1.00 22.87                         ATOM 2217 O GLY A 286 0 24.406 8.418 4.197 1.00 23.06                         ATOM 2218 N ALA A 287 0 23.504 10.076 5.423 1.00 22.81                        ATOM 2219 CA ALA A 287 0 22.176 9.449 5.364 1.00 21.50                        ATOM 2220 C ALA A 287 0 21.482 9.880 4.079 1.00 20.58                         ATOM 2221 O ALA A 287 0 21.647 11.032 3.629 1.00 19.44                        ATOM 2222 CB ALA A 287 0 21.340 9.890 6.562 1.00 21.34                        ATOM 2223 N ALA A 288 0 20.632 9.041 3.523 1.00 21.20                         ATOM 2224 CA ALA A 288 0 19.899 9.450 2.310 1.00 23.46                        ATOM 2225 C ALA A 288 0 18.965 10.629 2.513 1.00 24.70                        ATOM 2226 O ALA A 288 0 18.494 10.929 3.621 1.00 25.30                        ATOM 2227 CB ALA A 288 0 19.012 8.298 1.827 1.00 24.84                        ATOM 2228 N ASN A 289 0 18.638 11.300 1.411 1.00 25.98                        ATOM 2229 CA ASN A 289 0 17.674 12.398 1.439 1.00 27.16                       ATOM 2230 C ASN A 289 0 16.303 11.707 1.505 1.00 27.36                        ATOM 2231 O ASN A 289 0 15.761 11.330 0.477 1.00 27.56                        ATOM 2232 CB ASN A 289 0 17.784 13.250 0.189 1.00 29.01                       ATOM 2233 CG ASN A 289 0 18.808 14.364 0.299 1.00 30.44                       ATOM 2234 OD1 ASN A 289 0 20.005 14.168 0.545 1.00 30.40                      ATOM 2235 ND2 ASN A 289 0 18.340 15.591 0.121 1.00 31.98                      ATOM 2236 N ALA A 290 0 15.837 11.426 2.703 1.00 25.22                        ATOM 2237 CA ALA A 290 0 14.600 10.727 2.955 1.00 25.09                       ATOM 2238 C ALA A 290 0 14.087 11.057 4.363 1.00 22.98                        ATOM 2239 O ALA A 290 0 14.830 11.555 5.205 1.00 22.02                        ATOM 2240 CB ALA A 290 0 14.764 9.210 2.823 1.00 24.89                        ATOM 2241 N ASP A 291 0 12.822 10.718 4.597 1.00 21.88                        ATOM 2242 CA ASP A 291 0 12.223 10.985 5.907 1.00 21.71                       ATOM 2243 C ASP A 291 0 12.724 9.965 6.916 1.00 18.93                         ATOM 2244 O ASP A 291 0 12.911 8.814 6.596 1.00 19.66                         ATOM 2245 CB ASP A 291 0 10.695 10.862 5.834 1.00 22.63                       ATOM 2246 CG ASP A 291 0 10.088 12.005 5.076 1.00 25.41                       ATOM 2247 OD1 ASP A 291 0 10.781 12.988 4.735 1.00 27.11                      ATOM 2248 OD2 ASP A 291 0 8.885 11.932 4.812 1.00 27.47                       ATOM 2249 N PRO A 292 0 12.863 10.362 8.164 1.00 16.14                        ATOM 2250 CA PRO A 292 0 13.229 9.473 9.230 1.00 15.27                        ATOM 2251 C PRO A 292 0 12.087 8.484 9.389 1.00 19.40                         ATOM 2252 O PRO A 292 0 10.925 8.785 9.063 1.00 20.36                         ATOM 2253 CB PRO A 292 0 13.257 10.335 10.511 1.00 14.68                      ATOM 2254 CG PRO A 292 0 13.291 11.739 9.941 1.00 14.39                       ATOM 2255 CD PRO A 292 0 12.606 11.735 8.593 1.00 14.02                       ATOM 2256 N THR A 293 0 12.357 7.361 10.024 1.00 19.91                        ATOM 2257 CA THR A 293 0 11.360 6.379 10.373 1.00 20.62                       ATOM 2258 C THR A 293 0 11.589 6.055 11.847 1.00 20.83                        ATOM 2259 O THR A 293 0 11.323 4.943 12.287 1.00 23.91                        ATOM 2260 CB THR A 293 0 11.556 5.088 9.557 1.00 23.41                        ATOM 2261 OG1 THR A 293 0 12.874 4.577 9.836 1.00 24.50                       ATOM 2262 CG2 THR A 293 0 11.438 5.341 8.058 1.00 23.72                       ATOM 2263 N THR A 294 0 12.172 6.958 12.624 1.00 19.30                        ATOM 2264 CA THR A 294 0 12.440 6.634 14.017 1.00 19.42                       ATOM 2265 C THR A 294 0 11.214 6.896 14.878 1.00 20.66                        ATOM 2266 O THR A 294 0 10.240 7.485 14.411 1.00 19.89                        ATOM 2267 CB THR A 294 0 13.565 7.548 14.553 1.00 19.28                       ATOM 2268 OG1 THR A 294 0 13.174 8.889 14.251 1.00 17.55                      ATOM 2269 CG2 THR A 294 0 14.860 7.214 13.822 1.00 19.27                      ATOM 2270 N SER A 295 0 11.359 6.576 16.159 1.00 23.85                        ATOM 2271 CA SER A 295 0 10.274 6.851 17.095 1.00 27.18                       ATOM 2272 C SER A 295 0 10.781 7.484 18.375 1.00 27.92                        ATOM 2273 O SER A 295 0 11.900 7.292 18.844 1.00 27.09                        ATOM 2274 CB SER A 295 0 9.513 5.546 17.367 1.00 28.92                        ATOM 2275 OG SER A 295 0 10.389 4.761 18.160 1.00 33.04                       ATOM 2276 N ALA A 296 0 9.930 8.331 18.965 1.00 30.04                         ATOM 2277 CA ALA A 296 0 10.295 9.003 20.207 1.00 29.82                       ATOM 2278 C ALA A 296 0 10.552 8.011 21.327 1.00 30.83                        ATOM 2279 O ALA A 296 0 10.114 6.861 21.328 1.00 30.67                        ATOM 2280 CB ALA A 296 0 9.187 9.968 20.599 1.00 30.16                        ATOM 2281 N ASN A 297 0 11.286 8.489 22.328 1.00 31.65                        ATOM 2282 CA ASN A 297 0 11.543 7.750 23.549 1.00 32.16                       ATOM 2283 C ASN A 297 0 10.200 7.650 24.285 1.00 32.80                        ATOM 2284 O ASN A 297 0 9.492 8.616 24.565 1.00 31.30                         ATOM 2285 CB ASN A 297 0 12.522 8.497 24.443 1.00 33.07                       ATOM 2286 CG ASN A 297 0 12.869 7.742 25.706 1.00 35.21                       ATOM 2287 OD1 ASN A 297 0 12.116 6.965 26.284 1.00 35.45                      ATOM 2288 ND2 ASN A 297 0 14.106 7.982 26.162 1.00 37.10                      ATOM 2289 N PRO A 298 0 9.865 6.430 24.647 1.00 33.40                         ATOM 2290 CA PRO A 298 0 8.626 6.116 25.331 1.00 33.89                        ATOM 2291 C PRO A 298 0 8.580 6.690 26.732 1.00 32.60                         ATOM 2292 O PRO A 298 0 7.522 7.155 27.173 1.00 32.72                         ATOM 2293 CB PRO A 298 0 8.505 4.576 25.358 1.00 35.13                        ATOM 2294 CG PRO A 298 0 9.932 4.147 25.128 1.00 34.52                        ATOM 2295 CD PRO A 298 0 10.630 5.222 24.323 1.00 34.10                       ATOM 2296 N ASN A 299 0 9.689 6.721 27.461 1.00 29.60                         ATOM 2297 CA ASN A 299 0 9.701 7.229 28.834 1.00 28.47                        ATOM 2298 C ASN A 299 0 10.818 8.251 29.006 1.00 27.18                        ATOM 2299 O ASN A 299 0 11.906 7.967 29.528 1.00 25.69                        ATOM 2300 CB ASN A 299 0 9.964 6.017 29.747 1.00 29.50                        ATOM 2301 CG ASN A 299 0 8.907 4.935 29.673 1.00 32.34                        ATOM 2302 OD1 ASN A 299 0 9.090 3.873 29.075 1.00 33.50                       ATOM 2303 ND2 ASN A 299 0 7.735 5.182 30.251 1.00 33.04                       ATOM 2304 N PRO A 300 0 10.629 9.450 28.498 1.00 26.02                        ATOM 2305 CA PRO A 300 0 11.668 10.486 28.498 1.00 23.99                      ATOM 2306 C PRO A 300 0 11.987 11.054 29.860 1.00 21.16                       ATOM 2307 O PRO A 300 0 11.051 11.174 30.649 1.00 20.81                       ATOM 2308 CB PRO A 300 0 11.137 11.623 27.594 1.00 23.33                      ATOM 2309 CG PRO A 300 0 9.645 11.422 27.729 1.00 24.68                       ATOM 2310 CD PRO A 300 0 9.387 9.918 27.882 1.00 25.22                        ATOM 2311 N ALA A 301 0 13.242 11.361 30.179 1.00 19.17                       ATOM 2312 CA ALA A 301 0 13.538 12.139 31.410 1.00 17.57                      ATOM 2313 C ALA A 301 0 13.159 13.588 31.084 1.00 16.53                       ATOM 2314 O ALA A 301 0 13.613 14.235 30.131 1.00 16.24                       ATOM 2315 CB ALA A 301 0 15.006 11.982 31.774 1.00 17.17                      ATOM 2316 N GLN A 302 0 12.139 14.131 31.723 1.00 18.15                       ATOM 2317 CA GLN A 302 0 11.580 15.446 31.441 1.00 19.34                      ATOM 2318 C GLN A 302 0 12.335 16.580 32.124 1.00 19.16                       ATOM 2319 O GLN A 302 0 12.577 16.444 33.324 1.00 19.07                       ATOM 2320 CB GLN A 302 0 10.122 15.483 31.937 1.00 19.10                      ATOM 2321 CG GLN A 302 0 9.304 16.666 31.478 1.00 20.55                       ATOM 2322 CD GLN A 302 0 8.960 16.738 30.009 1.00 20.18                       ATOM 2323 OE1 GLN A 302 0 8.843 15.721 29.331 1.00 22.29                      ATOM 2324 NE2 GLN A 302 0 8.813 17.936 29.436 1.00 18.46                      ATOM 2325 N LEU A 303 0 12.629 17.681 31.444 1.00 17.92                       ATOM 2326 CA LEU A 303 0 13.241 18.824 32.139 1.00 17.32                      ATOM 2327 C LEU A 303 0 12.316 19.357 33.232 1.00 17.65                       ATOM 2328 O LEU A 303 0 11.140 19.664 33.021 1.00 17.55                       ATOM 2329 CB LEU A 303 0 13.489 19.988 31.168 1.00 15.14                      ATOM 2330 CG LEU A 303 0 13.919 21.317 31.797 1.00 16.94                      ATOM 2331 CD1 LEU A 303 0 15.262 21.146 32.504 1.00 17.30                     ATOM 2332 CD2 LEU A 303 0 13.988 22.432 30.764 1.00 12.82                     ATOM 2333 N ASN A 304 0 12.868 19.580 34.399 1.00 17.34                       ATOM 2334 CA ASN A 304 0 12.199 20.212 35.531 1.00 19.12                      ATOM 2335 C ASN A 304 0 13.071 21.435 35.833 1.00 19.06                       ATOM 2336 O ASN A 304 0 14.265 21.349 36.122 1.00 20.37                       ATOM 2337 CB ASN A 304 0 12.073 19.244 36.704 1.00 22.16                      ATOM 2338 CG ASN A 304 0 11.748 19.900 38.024 1.00 25.02                      ATOM 2339 OD1 ASN A 304 0 11.506 21.111 38.146 1.00 26.72                     ATOM 2340 ND2 ASN A 304 0 11.766 19.133 39.114 1.00 25.99                     ATOM 2341 N GLU A 305 0 12.541 22.629 35.662 1.00 17.64                       ATOM 2342 CA GLU A 305 0 13.204 23.890 35.840 1.00 16.64                      ATOM 2343 C GLU A 305 0 13.884 23.977 37.194 1.00 16.06                       ATOM 2344 O GLU A 305 0 14.965 24.564 37.208 1.00 14.78                       ATOM 2345 CB GLU A 305 0 12.286 25.085 35.567 1.00 15.91                      ATOM 2346 CG GLU A 305 0 12.898 26.484 35.831 1.00 14.81                      ATOM 2347 CD GLU A 305 0 11.794 27.546 35.666 1.00 15.72                      ATOM 2348 OE1 GLU A 305 0 11.584 28.026 34.527 1.00 14.63                     ATOM 2349 OE2 GLU A 305 0 11.154 27.861 36.685 1.00 13.05                     ATOM 2350 N ALA A 306 0 13.416 23.432 38.298 1.00 15.83                       ATOM 2351 CA ALA A 306 0 14.131 23.509 39.565 1.00 17.92                      ATOM 2352 C ALA A 306 0 15.437 22.682 39.532 1.00 18.62                       ATOM 2353 O ALA A 306 0 16.213 22.867 40.464 1.00 18.37                       ATOM 2354 CB ALA A 306 0 13.283 22.993 40.711 1.00 16.23                      ATOM 2355 N ASP A 307 0 15.721 21.860 38.523 1.00 18.04                       ATOM 2356 CA ASP A 307 0 16.988 21.164 38.409 1.00 18.68                      ATOM 2357 C ASP A 307 0 18.035 22.039 37.707 1.00 19.89                       ATOM 2358 O ASP A 307 0 19.239 21.695 37.739 1.00 20.36                       ATOM 2359 CB ASP A 307 0 16.904 19.863 37.592 1.00 17.64                      ATOM 2360 CG ASP A 307 0 15.980 18.873 38.290 1.00 18.17                      ATOM 2361 OD1 ASP A 307 0 15.918 18.919 39.535 1.00 18.27                     ATOM 2362 OD2 ASP A 307 0 15.311 18.094 37.592 1.00 17.32                     ATOM 2363 N LEU A 308 0 17.583 23.110 37.052 1.00 16.43                       ATOM 2364 CA LEU A 308 0 18.581 23.962 36.377 1.00 16.80                      ATOM 2365 C LEU A 308 0 19.327 24.827 37.384 1.00 16.94                       ATOM 2366 O LEU A 308 0 18.784 25.320 38.380 1.00 17.28                       ATOM 2367 CB LEU A 308 0 17.925 24.775 35.257 1.00 12.52                      ATOM 2368 CG LEU A 308 0 17.436 23.936 34.073 1.00 12.15                      ATOM 2369 CD1 LEU A 308 0 16.692 24.834 33.101 1.00 11.67                     ATOM 2370 CD2 LEU A 308 0 18.547 23.186 33.341 1.00 12.23                     ATOM 2371 N HIS A 309 0 20.640 24.968 37.243 1.00 18.01                       ATOM 2372 CA HIS A 309 0 21.430 25.802 38.158 1.00 18.47                      ATOM 2373 C HIS A 309 0 22.328 26.770 37.394 1.00 17.36                       ATOM 2374 O HIS A 309 0 23.015 26.378 36.459 1.00 17.82                       ATOM 2375 CB HIS A 309 0 22.267 24.997 39.140 1.00 18.51                      ATOM 2376 CG HIS A 309 0 21.470 24.052 39.965 1.00 20.71                      ATOM 2377 ND1 HIS A 309 0 21.526 22.684 39.790 1.00 21.77                     ATOM 2378 CD2 HIS A 309 0 20.578 24.285 40.956 1.00 22.07                     ATOM 2379 CE1 HIS A 309 0 20.701 22.115 40.657 1.00 22.85                     ATOM 2380 NE2 HIS A 309 0 20.120 23.059 41.377 1.00 22.67                     ATOM 2381 N ALA A 310 0 22.352 28.005 37.837 1.00 17.27                       ATOM 2382 CA ALA A 310 0 23.173 29.068 37.228 1.00 17.74                      ATOM 2383 C ALA A 310 0 24.663 28.775 37.342 1.00 18.13                       ATOM 2384 O ALA A 310 0 25.103 28.233 38.369 1.00 19.61                       ATOM 2385 CB ALA A 310 0 22.869 30.356 37.985 1.00 16.92                      ATOM 2386 N LEU A 311 0 25.427 29.021 36.304 1.00 19.30                       ATOM 2387 CA LEU A 311 0 26.856 28.762 36.277 1.00 20.71                      ATOM 2388 C LEU A 311 0 27.655 29.922 36.881 1.00 22.67                       ATOM 2389 O LEU A 311 0 28.581 29.788 37.682 1.00 23.06                       ATOM 2390 CB LEU A 311 0 27.305 28.591 34.817 1.00 20.57                      ATOM 2391 CG LEU A 311 0 28.796 28.196 34.684 1.00 21.52                      ATOM 2392 CD1 LEU A 311 0 28.993 26.783 35.229 1.00 20.80                     ATOM 2393 CD2 LEU A 311 0 29.319 28.282 33.254 1.00 20.17                     ATOM 2394 N ILE A 312 0 27.333 31.142 36.449 1.00 23.42                       ATOM 2395 CA ILE A 312 0 28.092 32.311 36.899 1.00 24.86                      ATOM 2396 C ILE A 312 0 27.337 33.157 37.914 1.00 26.54                       ATOM 2397 O ILE A 312 0 26.154 33.467 37.739 1.00 25.31                       ATOM 2398 CB ILE A 312 0 28.397 33.179 35.670 1.00 24.45                      ATOM 2399 CG1 ILE A 312 0 28.998 32.330 34.576 1.00 25.60                     ATOM 2400 CG2 ILE A 312 0 29.261 34.373 36.075 1.00 26.44                     ATOM 2401 CD1 ILE A 312 0 30.462 32.026 34.512 1.00 24.51                     ATOM 2402 N ASP A 313 0 28.008 33.523 39.003 1.00 28.70                       ATOM 2403 CA ASP A 313 0 27.432 34.339 40.071 1.00 30.99                      ATOM 2404 C ASP A 313 0 26.065 33.763 40.417 1.00 29.83                       ATOM 2405 O ASP A 313 0 25.024 34.385 40.235 1.00 28.51                       ATOM 2406 CB ASP A 313 0 27.266 35.777 39.576 1.00 35.88                      ATOM 2407 CG ASP A 313 0 28.532 36.505 39.187 1.00 40.21                      ATOM 2408 OD1 ASP A 313 0 29.577 36.243 39.847 1.00 42.99                     ATOM 2409 OD2 ASP A 313 0 28.525 37.346 38.252 1.00 40.95                     ATOM 2410 N PRO A 314 0 26.041 32.517 40.863 1.00 28.77                       ATOM 2411 CA PRO A 314 0 24.841 31.743 41.074 1.00 27.80                      ATOM 2412 C PRO A 314 0 23.865 32.198 42.137 1.00 26.49                       ATOM 2413 O PRO A 314 0 22.671 31.857 42.032 1.00 27.17                       ATOM 2414 CB PRO A 314 0 25.297 30.311 41.479 1.00 27.61                      ATOM 2415 CG PRO A 314 0 26.711 30.573 41.929 1.00 29.37                      ATOM 2416 CD PRO A 314 0 27.248 31.726 41.111 1.00 28.10                      ATOM 2417 N ALA A 315 0 24.364 32.818 43.206 1.00 23.45                       ATOM 2418 CA ALA A 315 0 23.505 33.092 44.336 1.00 22.34                      ATOM 2419 C ALA A 315 0 22.414 34.111 44.008 1.00 22.46                       ATOM 2420 O ALA A 315 0 22.678 35.127 43.370 1.00 22.52                       ATOM 2421 CB ALA A 315 0 24.294 33.617 45.532 1.00 21.68                      ATOM 2422 N ALA A 316 0 21.226 33.838 44.534 1.00 20.85                       ATOM 2423 CA ALA A 316 0 20.133 34.805 44.422 1.00 20.78                      ATOM 2424 C ALA A 316 0 20.547 36.010 45.271 1.00 20.55                       ATOM 2425 O ALA A 316 0 21.143 35.846 46.333 1.00 21.47                       ATOM 2426 CB ALA A 316 0 18.897 34.166 45.043 1.00 18.32                      ATOM 2427 N PRO A 317 0 20.237 37.212 44.864 1.00 20.84                       ATOM 2428 CA PRO A 317 0 20.539 38.410 45.634 1.00 20.82                      ATOM 2429 C PRO A 317 0 19.766 38.449 46.945 1.00 20.96                       ATOM 2430 O PRO A 317 0 18.668 37.885 47.030 1.00 21.42                       ATOM 2431 CB PRO A 317 0 20.064 39.590 44.758 1.00 21.64                      ATOM 2432 CG PRO A 317 0 19.178 38.938 43.746 1.00 21.69                      ATOM 2433 CD PRO A 317 0 19.517 37.466 43.619 1.00 20.10                      ATOM 2434 N GLY A 318 0 20.269 39.080 47.988 1.00 20.69                       ATOM 2435 CA GLY A 318 0 19.533 39.282 49.225 1.00 21.68                      ATOM 2436 C GLY A 318 0 19.631 38.218 50.283 1.00 22.93                       ATOM 2437 O GLY A 318 0 20.344 37.221 50.101 1.00 23.87                       ATOM 2438 N ILE A 319 0 18.895 38.398 51.368 1.00 22.20                       ATOM 2439 CA ILE A 319 0 18.879 37.432 52.454 1.00 24.16                      ATOM 2440 C ILE A 319 0 18.169 36.189 51.956 1.00 25.28                       ATOM 2441 O ILE A 319 0 17.071 36.271 51.405 1.00 26.26                       ATOM 2442 CB ILE A 319 0 18.208 38.030 53.704 1.00 24.54                      ATOM 2443 CG1 ILE A 319 0 19.075 39.176 54.213 1.00 25.08                     ATOM 2444 CG2 ILE A 319 0 17.944 37.012 54.793 1.00 24.03                     ATOM 2445 CD1 ILE A 319 0 18.262 40.183 55.006 1.00 27.56                     ATOM 2446 N PRO A 320 0 18.762 35.030 52.159 1.00 26.23                       ATOM 2447 CA PRO A 320 0 18.273 33.748 51.684 1.00 26.64                      ATOM 2448 C PRO A 320 0 17.105 33.172 52.453 1.00 26.74                       ATOM 2449 O PRO A 320 0 17.140 32.025 52.896 1.00 27.54                       ATOM 2450 CB PRO A 320 0 19.501 32.801 51.772 1.00 27.16                      ATOM 2451 CG PRO A 320 0 20.216 33.388 52.985 1.00 25.20                      ATOM 2452 CD PRO A 320 0 20.061 34.891 52.837 1.00 25.62                      ATOM 2453 N THR A 321 0 16.022 33.909 52.611 1.00 27.35                       ATOM 2454 CA THR A 321 0 14.820 33.550 53.329 1.00 28.07                      ATOM 2455 C THR A 321 0 13.632 34.190 52.603 1.00 27.48                       ATOM 2456 O THR A 321 0 13.597 35.383 52.302 1.00 27.13                       ATOM 2457 CB THR A 321 0 14.824 34.085 54.780 1.00 29.87                      ATOM 2458 OG1 THR A 321 0 15.957 33.582 55.511 1.00 31.85                     ATOM 2459 CG2 THR A 321 0 13.548 33.687 55.507 1.00 31.06                     ATOM 2460 N PRO A 322 0 12.630 33.378 52.326 1.00 26.63                       ATOM 2461 CA PRO A 322 0 11.428 33.824 51.637 1.00 25.91                      ATOM 2462 C PRO A 322 0 10.892 35.072 52.313 1.00 25.37                       ATOM 2463 O PRO A 322 0 10.945 35.194 53.542 1.00 25.02                       ATOM 2464 CB PRO A 322 0 10.456 32.638 51.661 1.00 26.11                      ATOM 2465 CG PRO A 322 0 11.370 31.477 51.931 1.00 26.67                      ATOM 2466 CD PRO A 322 0 12.592 31.961 52.691 1.00 26.21                      ATOM 2467 N GLY A 323 0 10.432 36.075 51.573 1.00 24.30                       ATOM 2468 CA GLY A 323 0 9.943 37.288 52.197 1.00 24.13                       ATOM 2469 C GLY A 323 0 11.013 38.161 52.842 1.00 25.48                       ATOM 2470 O GLY A 323 0 10.603 39.128 53.512 1.00 25.28                       ATOM 2471 N ALA A 324 0 12.320 37.959 52.688 1.00 24.80                       ATOM 2472 CA ALA A 324 0 13.278 38.831 53.377 1.00 24.61                      ATOM 2473 C ALA A 324 0 14.034 39.773 52.451 1.00 23.92                       ATOM 2474 O ALA A 324 0 15.148 40.225 52.748 1.00 24.53                       ATOM 2475 CB ALA A 324 0 14.255 38.012 54.204 1.00 23.79                      ATOM 2476 N ALA A 325 0 13.423 40.081 51.315 1.00 22.22                       ATOM 2477 CA ALA A 325 0 14.033 40.985 50.341 1.00 20.42                      ATOM 2478 C ALA A 325 0 13.825 42.423 50.803 1.00 19.97                       ATOM 2479 O ALA A 325 0 12.987 42.648 51.677 1.00 18.14                       ATOM 2480 CB ALA A 325 0 13.272 40.763 49.018 1.00 19.40                      ATOM 2481 N ASP A 326 0 14.422 43.421 50.161 1.00 20.69                       ATOM 2482 CA ASP A 326 0 14.141 44.804 50.529 1.00 22.54                      ATOM 2483 C ASP A 326 0 12.702 45.158 50.220 1.00 22.83                       ATOM 2484 O ASP A 326 0 12.015 45.754 51.030 1.00 23.68                       ATOM 2485 CB ASP A 326 0 15.089 45.767 49.789 1.00 22.32                      ATOM 2486 CG ASP A 326 0 16.494 45.378 50.238 1.00 23.83                      ATOM 2487 OD1 ASP A 326 0 16.650 45.284 51.475 1.00 24.78                     ATOM 2488 OD2 ASP A 326 0 17.393 45.171 49.409 1.00 24.90                     ATOM 2489 N VAL A 327 0 12.254 44.821 49.026 1.00 24.29                       ATOM 2490 CA VAL A 327 0 10.914 45.064 48.503 1.00 23.57                      ATOM 2491 C VAL A 327 0 10.246 43.721 48.170 1.00 23.46                       ATOM 2492 O VAL A 327 0 10.785 42.933 47.386 1.00 22.62                       ATOM 2493 CB VAL A 327 0 10.946 45.898 47.220 1.00 24.70                      ATOM 2494 CG1 VAL A 327 0 9.554 46.274 46.751 1.00 24.11                      ATOM 2495 CG2 VAL A 327 0 11.773 47.173 47.420 1.00 26.30                     ATOM 2496 N ASN A 328 0 9.113 43.463 48.811 1.00 21.44                        ATOM 2497 CA ASN A 328 0 8.390 42.212 48.717 1.00 23.21                       ATOM 2498 C ASN A 328 0 6.986 42.410 48.158 1.00 23.12                        ATOM 2499 O ASN A 328 0 6.140 43.030 48.799 1.00 22.76                        ATOM 2500 CB ASN A 328 0 8.223 41.603 50.121 1.00 23.09                       ATOM 2501 CG ASN A 328 0 9.569 41.204 50.693 1.00 24.61                       ATOM 2502 OD1 ASN A 328 0 10.181 40.188 50.295 1.00 25.87                     ATOM 2503 ND2 ASN A 328 0 10.017 42.029 51.617 1.00 21.47                     ATOM 2504 N LEU A 329 0 6.776 42.000 46.923 1.00 23.14                        ATOM 2505 CA LEU A 329 0 5.497 42.179 46.268 1.00 24.23                       ATOM 2506 C LEU A 329 0 4.859 40.822 45.953 1.00 25.21                        ATOM 2507 O LEU A 329 0 5.489 39.876 45.469 1.00 24.20                        ATOM 2508 CB LEU A 329 0 5.622 42.963 44.948 1.00 24.33                       ATOM 2509 CG LEU A 329 0 6.369 44.279 45.082 1.00 26.30                       ATOM 2510 CD1 LEU A 329 0 6.778 44.884 43.757 1.00 26.24                      ATOM 2511 CD2 LEU A 329 0 5.550 45.249 45.913 1.00 27.07                      ATOM 2512 N ARG A 330 0 3.562 40.806 46.204 1.00 25.13                        ATOM 2513 CA ARG A 330 0 2.740 39..641 45.899 1.00 27.48                      ATOM 2514 C ARG A 330 0 1.628 40.116 44.965 1.00 27.52                        ATOM 2515 O ARG A 330 0 0.988 41.132 45.257 1.00 27.17                        ATOM 2516 CB ARG A 330 0 2.200 39.017 47.166 1.00 29.82                       ATOM 2517 CG ARG A 330 0 1.351 37.794 46.932 1.00 33.18                       ATOM 2518 CD ARG A 330 0 0.880 37.251 48.284 1.00 37.06                       ATOM 2519 NE ARG A 330 0 0.305 35.914 48.038 1.00 40.34                       ATOM 2520 CZ ARG A 330 0 1.009 34.803 48.298 1.00 40.82                       ATOM 2521 NH1 ARG A 330 0 2.229 34.903 48.812 1.00 40.36                      ATOM 2522 NH2 ARG A 330 0 0.415 33.642 48.040 1.00 41.33                      ATOM 2523 N PHE A 331 0 1.507 39.481 43.795 1.00 25.88                        ATOM 2524 CA PHE A 331 0 0.475 39.937 42.855 1.00 25.87                       ATOM 2525 C PHE A 331 0 -0.657 3.8.919 42.779 1.00 25.94                      ATOM 2526 O PHE A 331 0 -0.441 37.697 42.824 1.00 24.61                       ATOM 2527 CB PHE A 331 0 1.102 40.269 41.511 1.00 25.94                       ATOM 2528 CG PHE A 331 0 1.884 41.565 41.496 1.00 28.66                       ATOM 2529 CD1 PHE A 331 0 1.282 42.782 41.759 1.00 28.04                      ATOM 2530 CD2 PHE A 331 0 3.246 41.569 41.214 1.00 29.71                      ATOM 2531 CE1 PHE A 331 0 1.988 43.963 41.744 1.00 29.21                      ATOM 2532 CE2 PHE A 331 0 3.975 42.753 41.181 1.00 30.61                      ATOM 2533 CZ PHE A 331 0 3.348 43.965 41.453 1.00 30.66                       ATOM 2534 N GLN A 332 0 -1.873 39.446 42.676 1.00 25.58                       ATOM 2535 CA GLN A 332 0 -3.085 38.628 42.608 1.00 26.60                      ATOM 2536 C GLN A 332 0 -3.672 38.698 41.203 1.00 23.61                       ATOM 2537 O GLN A 332 0 -4.136 39.739 40.755 1.00 21.73                       ATOM 2538 CB GLN A 332 0 -4.110 39.094 43.630 1.00 30.32                      ATOM 2539 CG GLN A 332 0 -5.412 38.299 43.642 1.00 35.72                      ATOM 2540 CD GLN A 332 0 -5.199 36.961 44.325 1.00 39.98                      ATOM 2541 OE1 GLN A 332 0 -5.859 35.961 44.007 1.00 42.32                     ATOM 2542 NE2 GLN A 332 0 -4.257 36.915 45.270 1.00 42.27                     ATOM 2543 N LEU A 333 0 -3.612 37.576 40.504 1.00 23.60                       ATOM 2544 CA LEU A 333 0 -4.105 37.565 39.118 1.00 26.25                      ATOM 2545 C LEU A 333 0 -5.627 37.373 39.123 1.00 26.55                       ATOM 2546 O LEU A 333 0 -6.107 36.655 39.998 1.00 25.70                       ATOM 2547 CB LEU A 333 0 -3.424 36.465 38.304 1.00 25.25                      ATOM 2548 CG LEU A 333 0 -1.919 36.608 38.052 1.00 25.72                      ATOM 2549 CD1 LEU A 333 0 -1.431 35.565 37.067 1.00 23.66                     ATOM 2550 CD2 LEU A 333 0 -1.551 38.000 37.558 1.00 25.25                     ATOM 2551 N GLY A 334 0 -6.327 37.976 38.188 1.00 27.85                       ATOM 2552 CA GLY A 334 0 -7.770 37.782 38.118 1.00 29.96                      ATOM 2553 C GLY A 334 0 -8.253 37.802 36.672 1.00 32.36                       ATOM 2554 O GLY A 334 0 -7.559 38.175 35.719 1.00 30.74                       ATOM 2555 N PHE A 335 0 -9.502 37.377 36.544 1.00 34.76                       ATOM 2556 CA PHE A 335 0 -10.181 37.360 35.260 1.00 38.54                     ATOM 2557 C PHE A 335 0 -11.625 37.806 35.514 1.00 41.05                      ATOM 2558 O PHE A 335 0 -12.443 37.028 36.021 1.00 41.53                      ATOM 2559 CB PHE A 335 0 -10.183 36.003 34.586 1.00 39.00                     ATOM 2560 CG PHE A 335 0 -10.772 36.105 33.197 1.00 40.61                     ATOM 2561 CD1 PHE A 335 0 -10.052 36.686 32.175 1.00 40.45                    ATOM 2562 CD2 PHE A 335 0 -12.045 35.614 32.942 1.00 41.39                    ATOM 2563 CE1 PHE A 335 0 -10.580 36.778 30.901 1.00 40.81                    ATOM 2564 CE2 PHE A 335 0 -12.588 35.697 31.671 1.00 41.51                    ATOM 2565 CZ PHE A 335 0 -11.849 36.281 30.652 1.00 41.87                     ATOM 2566 N SER A 336 0 -11.861 39.075 35.193 1.00 42.39                      ATOM 2567 CA SER A 336 0 -13.203 39.582 35.445 1.00 44.12                     ATOM 2568 C SER A 336 0 -13.704 40.525 34.370 1.00 44.31                      ATOM 2569 O SER A 336 0 -13.028 41.440 33.903 1.00 44.49                      ATOM 2570 CB SER A 336 0 -13.214 40.206 36.842 1.00 45.46                     ATOM 2571 OG SER A 336 0 -13.727 39.233 37.758 1.00 47.11                     ATOM 2572 N GLY A 337 0 -14.963 40.267 33.983 1.00 44.12                      ATOM 2573 CA GLY A 337 0 -15.630 41.067 32.959 1.00 41.89                     ATOM 2574 C GLY A 337 0 -14.963 40.920 31.608 1.00 40.08                      ATOM 2575 O GLY A 337 0 -14.712 41.891 30.888 1.00 41.35                      ATOM 2576 N GLY A 338 0 -14.583 39.699 31.263 1.00 39.12                      ATOM 2577 CA GLY A 338 0 -13.899 39.364 30.034 1.00 36.11                     ATOM 2578 C GLY A 338 0 -12.503 39.970 29.929 1.00 34.97                      ATOM 2579 O GLY A 338 0 -12.005 40.116 28.806 1.00 33.64                      ATOM 2580 N ARG A 339 0 -11.885 40.355 31.048 1.00 33.21                      ATOM 2581 CA ARG A 339 0 -10.538 40.916 30.982 1.00 32.04                     ATOM 2582 C ARG A 339 0 -9.724 40.397 32.164 1.00 29.23                       ATOM 2583 O ARG A 339 0 -10.260 40.053 33.210 1.00 26.38                      ATOM 2584 CB ARG A 339 0 -10.495 42.419 30.845 1.00 36.52                     ATOM 2585 CG ARG A 339 0 -11.291 43.281 31.790 1.00 42.08                     ATOM 2586 CD ARG A 339 0 -11.895 44.502 31.127 1.00 45.03                     ATOM 2587 NE ARG A 339 0 -11.046 45.380 30.351 1.00 47.77                     ATOM 2588 CZ ARG A 339 0 -10.635 46.616 30.664 1.00 49.55                     ATOM 2589 NH1 ARG A 339 0 -10.935 47.242 31.799 1.00 49.60                    ATOM 2590 NH2 ARG A 339 0 -9.862 47.295 29.805 1.00 49.96                     ATOM 2591 N PHE A 340 0 -8.425 40.181 31.900 1.00 25.50                       ATOM 2592 CA PHE A 340 0 -7.526 39.713 32.938 1.00 22.68                      ATOM 2593 C PHE A 340 0 -7.171 40.945 33.774 1.00 22.15                       ATOM 2594 O PHE A 340 0 -7.069 42.069 33.266 1.00 21.26                       ATOM 2595 CB PHE A 340 0 -6.210 39.135 32.397 1.00 22.39                      ATOM 2596 CG PHE A 340 0 -6.333 37.792 31.736 1.00 20.74                      ATOM 2597 CD1 PHE A 340 0 -6.338 37.710 30.357 1.00 20.97                     ATOM 2598 CD2 PHE A 340 0 -6.448 36.644 32.468 1.00 21.19                     ATOM 2599 CE1 PHE A 340 0 -6.449 36.488 29.721 1.00 21.61                     ATOM 2600 CE2 PHE A 340 0 -6.585 35.408 31.826 1.00 22.99                     ATOM 2601 CZ PHE A 340 0 -6.578 35.334 30.444 1.00 19.90                      ATOM 2602 N THR A 341 0 -7.000 40.736 35.069 1.00 20.76                       ATOM 2603 CA THR A 341 0 -6.605 41.879 35.889 1.00 21.55                      ATOM 2604 C THR A 341 0 -5.400 41.509 36.759 1.00 21.00                       ATOM 2605 O THR A 341 0 -5.236 40.329 37.089 1.00 20.70                       ATOM 2606 CB THR A 341 0 -7.757 42.255 36.853 1.00 21.12                      ATOM 2607 OG1 THR A 341 0 -8.014 41.102 37.668 1.00 21.26                     ATOM 2608 CG2 THR A 341 0 -9.050 42.630 36.150 1.00 21.74                     ATOM 2609 N ILE A 342 0 -4.750 42.529 37.308 1.00 20.28                       ATOM 2610 CA ILE A 342 0 -3.739 42.273 38.333 1.00 20.34                      ATOM 2611 C ILE A 342 0 -4.026 43.212 39.496 1.00 18.92                       ATOM 2612 O ILE A 342 0 -4.004 44.437 39.327 1.00 16.42                       ATOM 2613 CB ILE A 342 0 -2.306 42.439 37.820 1.00 21.04                      ATOM 2614 CG1 ILE A 342 0 -1.337 42.721 38.988 1.00 21.39                     ATOM 2615 CG2 ILE A 342 0 -2.250 43.540 36.800 1.00 24.57                     ATOM 2616 CD1 ILE A 342 0 -0.260 41.661 38.949 1.00 24.53                     ATOM 2617 N ASN A 343 0 -4.282 42.601 40.650 1.00 17.77                       ATOM 2618 CA ASN A 343 0 -4.702 43.413 41.782 1.00 21.51                      ATOM 2619 C ASN A 343 0 -5.881 44.287 41.394 1.00 21.43                       ATOM 2620 O ASN A 343 0 -5.903 45.495 41.598 1.00 20.26                       ATOM 2621 CB ASN A 343 0 -3.513 44.231 42.356 1.00 22.34                      ATOM 2622 CG ASN A 343 0 -2.685 43.190 43.073 1.00 25.38                      ATOM 2623 OD1 ASN A 343 0 -2.075 42.218 42.598 1.00 26.90                     ATOM 2624 ND2 ASN A 343 0 -2.652 43.238 44.425 1.00 25.34                     ATOM 2625 N GLY A 344 0 -6.875 43.703 40.730 1.00 23.77                       ATOM 2626 CA GLY A 344 0 -8.078 44.406 40.324 1.00 25.28                      ATOM 2627 C GLY A 344 0 -7.954 45.280 39.111 1.00 26.82                       ATOM 2628 O GLY A 344 0 -9.029 45.728 38.672 1.00 29.56                       ATOM 2629 N THR A 345 0 -6.798 45.561 38.527 1.00 26.28                       ATOM 2630 CA THR A 345 0 -6.766 46.440 37.366 1.00 25.48                      ATOM 2631 C THR A 345 0 -6.343 45.703 36.109 1.00 26.49                       ATOM 2632 O THR A 345 0 -5.385 44.925 36.122 1.00 28.22                       ATOM 2633 CB THR A 345 0 -5.829 47.648 37.589 1.00 26.17                      ATOM 2634 OG1 THR A 345 0 -6.191 48.334 38.788 1.00 25.32                     ATOM 2635 CG2 THR A 345 0 -5.867 48.677 36.462 1.00 24.83                     ATOM 2636 N ALA A 346 0 -7.017 46.012 35.008 1.00 24.80                       ATOM 2637 CA ALA A 346 0 -6.768 45.491 33.688 1.00 23.82                      ATOM 2638 C ALA A 346 0 -5.862 46.511 32.997 1.00 23.77                       ATOM 2639 O ALA A 346 0 -6.098 47.711 33.088 1.00 22.93                       ATOM 2640 CB ALA A 346 0 -8.031 45.353 32.841 1.00 24.13                      ATOM 2641 N TYR A 347 0 -4.793 46.023 32.392 1.00 22.69                       ATOM 2642 CA TYR A 347 0 -3.862 46.949 31.792 1.00 22.75                      ATOM 2643 C TYR A 347 0 -4.483 47.532 30.527 1.00 23.42                       ATOM 2644 O TYR A 347 0 -4.954 46.753 29.709 1.00 22.19                       ATOM 2645 CB TYR A 347 0 -2.521 46.274 31.455 1.00 21.25                      ATOM 2646 CG TYR A 347 0 -1.584 47.221 30.732 1.00 18.93                      ATOM 2647 CD1 TYR A 347 0 -0.819 48.137 31.442 1.00 18.17                     ATOM 2648 CD2 TYR A 347 0 -1.473 47.176 29.353 1.00 19.30                     ATOM 2649 CE1 TYR A 347 0 0.034 49.003 30.763 1.00 18.37                      ATOM 2650 CE2 TYR A 347 0 -0.650 48.063 28.664 1.00 18.40                     ATOM 2651 CZ TYR A 347 0 0.102 48.962 29.394 1.00 18.99                       ATOM 2652 OH TYR A 347 0 0.947 49.802 28.706 1.00 19.65                       ATOM 2653 N GLU A 348 0 -4.378 48.833 30.359 1.00 25.22                       ATOM 2654 CA GLU A 348 0 -4.769 49.453 29.098 1.00 28.77                      ATOM 2655 C GLU A 348 0 -3.659 50.470 28.805 1.00 27.38                       ATOM 2656 O GLU A 348 0 -3.297 51.229 29.704 1.00 28.49                       ATOM 2657 CB GLU A 348 0 -6.114 50.134 29.110 1.00 32.95                      ATOM 2658 CG GLU A 348 0 -7.391 49.302 29.072 1.00 39.29                      ATOM 2659 CD GLU A 348 0 -8.562 50.170 29.559 1.00 43.20                      ATOM 2660 OE1 GLU A 348 0 -8.825 51.211 28.900 1.00 45.31                     ATOM 2661 OE2 GLU A 348 0 -9.175 49.855 30.601 1.00 44.11                     ATOM 2662 N SER A 349 0 -3.168 50.541 27.621 1.00 25.73                       ATOM 2663 CA SER A 349 0 -2.080 51.410 27.201 1.00 28.25                      ATOM 2664 C SER A 349 0 -2.401 52.887 27.194 1.00 28.71                       ATOM 2665 O SER A 349 0 -3.279 53.399 26.526 1.00 29.13                       ATOM 2666 CB SER A 349 0 -1.743 50.818 25.838 1.00 28.54                      ATOM 2667 OG SER A 349 0 -0.850 51.499 25.026 1.00 33.31                      ATOM 2668 N PRO A 350 0 -1.623 53.700 27.898 1.00 29.56                       ATOM 2669 CA PRO A 350 0 -1.770 55.145 27.997 1.00 28.53                      ATOM 2670 C PRO A 350 0 -1.480 55.825 26.679 1.00 28.01                       ATOM 2671 O PRO A 350 0 -0.787 55.217 25.856 1.00 26.93                       ATOM 2672 CB PRO A 350 0 -0.752 55.632 29.063 1.00 27.91                      ATOM 2673 CG PRO A 350 0 0.309 54.560 28.863 1.00 28.03                       ATOM 2674 CD PRO A 350 0 -0.461 53.245 28.688 1.00 28.76                      ATOM 2675 N SER A 351 0 -1.951 57.066 26.485 1.00 28.89                       ATOM 2676 CA SER A 351 0 -1.630 57.718 25.206 1.00 29.67                      ATOM 2677 C SER A 351 0 -0.213 58.287 25.257 1.00 27.67                       ATOM 2678 O SER A 351 0 0.320 58.524 24.177 1.00 28.18                        ATOM 2679 CB SER A 351 0 -2.566 58.860 24.790 1.00 31.71                      ATOM 2680 OG SER A 351 0 -2.793 59.679 25.938 1.00 34.19                      ATOM 2681 N VAL A 352 0 0.316 58.529 26.449 1.00 25.32                        ATOM 2682 CA VAL A 352 0 1.703 58.997 26.534 1.00 25.27                       ATOM 2683 C VAL A 352 0 2.503 57.872 27.211 1.00 23.63                        ATOM 2684 O VAL A 352 0 2.181 57.493 28.323 1.00 23.26                        ATOM 2685 CB VAL A 352 0 1.934 60.300 27.303 1.00 24.91                       ATOM 2686 CG1 VAL A 352 0 1.129 61.436 26.658 1.00 24.41                      ATOM 2687 CG2 VAL A 352 0 3.424 60.635 27.281 1.00 23.35                      ATOM 2688 N PRO A 353 0 3.498 57.375 26.510 1.00 22.39                        ATOM 2689 CA PRO A 353 0 4.342 56.300 26.983 1.00 21.86                       ATOM 2690 C PRO A 353 0 4.978 56.699 28.300 1.00 20.91                        ATOM 2691 O PRO A 353 0 5.393 57.852 28.483 1.00 21.91                        ATOM 2692 CB PRO A 353 0 5.417 56.054 25.916 1.00 23.95                       ATOM 2693 CG PRO A 353 0 5.181 57.123 24.878 1.00 23.79                       ATOM 2694 CD PRO A 353 0 3.882 57.848 25.180 1.00 23.03                       ATOM 2695 N THR A 354 0 5.043 55.778 29.234 1.00 18.66                        ATOM 2696 CA THR A 354 0 5.646 56.015 30.530 1.00 18.05                       ATOM 2697 C THR A 354 0 6.981 56.739 30.478 1.00 18.33                        ATOM 2698 O THR A 354 0 7.168 57.630 31.319 1.00 19.46                        ATOM 2699 CB THR A 354 0 5.871 54.661 31.242 1.00 17.10                       ATOM 2700 OG1 THR A 354 0 4.903 53.710 30.797 1.00 17.24                      ATOM 2701 CG2 THR A 354 0 5.772 54.852 32.741 1.00 16.43                      ATOM 2702 N LEU A 355 0 7.940 56.380 29.618 1.00 17.49                        ATOM 2703 CA LEU A 355 0 9.215 57.076 29.604 1.00 18.84                       ATOM 2704 C LEU A 355 0 9.013 58.579 29.284 1.00 19.80                        ATOM 2705 O LEU A 355 0 9.722 59.417 29.849 1.00 17.13                        ATOM 2706 CB LEU A 355 0 10.200 56.498 28.622 1.00 17.89                      ATOM 2707 CG LEU A 355 0 11.703 56.488 28.819 1.00 18.66                      ATOM 2708 CD1 LEU A 355 0 12.436 56.851 27.547 1.00 18.37                     ATOM 2709 CD2 LEU A 355 0 12.199 57.204 30.056 1.00 16.79                     ATOM 2710 N LEU A 356 0 8.134 58.883 28.328 1.00 20.48                        ATOM 2711 CA LEU A 356 0 7.812 60.274 27.993 1.00 21.62                       ATOM 2712 C LEU A 356 0 7.085 60.932 29.163 1.00 21.28                        ATOM 2713 O LEU A 356 0 7.497 62.042 29.506 1.00 22.01                        ATOM 2714 CB LEU A 356 0 7.028 60.474 26.700 1.00 22.08                       ATOM 2715 CG LEU A 356 0 6.850 61.939 26.239 1.00 23.98                       ATOM 2716 CD1 LEU A 356 0 8.157 62.709 26.207 1.00 23.11                      ATOM 2717 CD2 LEU A 356 0 6.191 61.985 24.864 1.00 24.74                      ATOM 2718 N GLN A 357 0 6.219 60.267 29.922 1.00 21.37                        ATOM 2719 CA GLN A 357 0 5.669 60.893 31.120 1.00 21.87                       ATOM 2720 C GLN A 357 0 6.759 61.254 32.128 1.00 24.12                        ATOM 2721 O GLN A 357 0 6.674 62.277 32.811 1.00 24.92                        ATOM 2722 CB GLN A 357 0 4.636 60.015 31.822 1.00 20.63                       ATOM 2723 CG GLN A 357 0 3.447 59.674 30.906 1.00 19.17                       ATOM 2724 CD GLN A 357 0 2.547 58.643 31.540 1.00 18.85                       ATOM 2725 OE1 GLN A 357 0 2.162 58.748 32.713 1.00 19.06                      ATOM 2726 NE2 GLN A 357 0 2.262 57.600 30.742 1.00 18.49                      ATOM 2727 N ILE A 358 0 7.735 60.371 32.346 1.00 25.66                        ATOM 2728 CA ILE A 358 0 8.822 60.651 33.263 1.00 26.19                       ATOM 2729 C ILE A 358 0 9.699 61.800 32.762 1.00 27.66                        ATOM 2730 O ILE A 358 0 9.940 62.725 33.551 1.00 26.65                        ATOM 2731 CB ILE A 358 0 9.692 59.420 33.578 1.00 24.79                       ATOM 2732 CG1 ILE A 358 0 8.807 58.395 34.304 1.00 24.09                      ATOM 2733 CG2 ILE A 358 0 10.865 59.841 34.451 1.00 23.78                     ATOM 2734 CD1 ILE A 358 0 9.251 56.954 34.234 1.00 23.34                      ATOM 2735 N MET A 359 0 10.054 61.844 31.486 1.00 29.63                       ATOM 2736 CA MET A 359 0 10.893 62.910 30.965 1.00 33.02                      ATOM 2737 C MET A 359 0 10.174 64.260 31.027 1.00 34.46                       ATOM 2738 O MET A 359 0 10.801 65.324 31.026 1.00 33.77                       ATOM 2739 CB MET A 359 0 11.346 62.664 29.537 1.00 35.67                      ATOM 2740 CG MET A 359 0 12.065 61.403 29.138 1.00 40.75                      ATOM 2741 SD MET A 359 0 13.764 61.153 29.671 1.00 44.90                      ATOM 2742 CE MET A 359 0 14.594 62.592 29.007 1.00 44.24                      ATOM 2743 N SER A 360 0 8.835 64.238 31.070 1.00 33.43                        ATOM 2744 CA SER A 360 0 8.024 65.430 31.088 1.00 32.92                       ATOM 2745 C SER A 360 0 7.761 65.995 32.474 1.00 33.24                        ATOM 2746 O SER A 360 0 6.989 66.966 32.556 1.00 34.08                        ATOM 2747 CB SER A 360 0 6.678 65.134 30.393 1.00 31.34                       ATOM 2748 OG SER A 360 0 6.928 65.109 28.996 1.00 31.06                       ATOM 2749 N GLY A 361 0 8.288 65.360 33.517 1.00 32.06                        ATOM 2750 CA GLY A 361 0 8.072 65.868 34.847 1.00 31.80                       ATOM 2751 C GLY A 361 0 7.487 64.955 35.880 1.00 32.48                        ATOM 2752 O GLY A 361 0 7.420 65.377 37.043 1.00 33.20                        ATOM 2753 N ALA A 362 0 6.991 63.769 35.535 1.00 33.69                        ATOM 2754 CA ALA A 362 0 6.406 62.926 36.601 1.00 35.10                       ATOM 2755 C ALA A 362 0 7.475 62.615 37.650 1.00 34.45                        ATOM 2756 O ALA A 362 0 8.598 62.306 37.286 1.00 33.60                        ATOM 2757 CB ALA A 362 0 5.789 61.658 36.043 1.00 34.88                       ATOM 2758 N GLN A 363 0 7.146 62.676 38.920 1.00 36.22                        ATOM 2759 CA GLN A 363 0 8.083 62.458 40.007 1.00 37.87                       ATOM 2760 C GLN A 363 0 7.776 61.189 40.787 1.00 37.20                        ATOM 2761 O GLN A 363 0 8.620 60.777 41.587 1.00 36.79                        ATOM 2762 CB GLN A 363 0 8.012 63.619 41.022 1.00 40.41                       ATOM 2763 CG GLN A 363 0 8.986 64.740 40.721 1.00 44.07                       ATOM 2764 CD GLN A 363 0 8.586 66.154 41.092 1.00 45.77                       ATOM 2765 OE1 GLN A 363 0 7.697 66.473 41.901 1.00 46.53                      ATOM 2766 NE2 GLN A 363 0 9.294 67.089 40.435 1.00 46.12                      ATOM 2767 N SER A 364 0 6.579 60.632 40.610 1.00 35.74                        ATOM 2768 CA SER A 364 0 6.249 59.434 41.381 1.00 34.54                       ATOM 2769 C SER A 364 0 5.225 58.588 40.653 1.00 34.32                        ATOM 2770 O SER A 364 0 4.605 59.037 39.692 1.00 33.71                        ATOM 2771 CB SER A 364 0 5.774 59.835 42.769 1.00 35.68                       ATOM 2772 OG SER A 364 0 4.396 60.095 42.928 1.00 35.86                       ATOM 2773 N ALA A 365 0 5.015 57.372 41.146 1.00 33.95                        ATOM 2774 CA ALA A 365 0 4.017 56.486 40.564 1.00 34.62                       ATOM 2775 C ALA A 365 0 2.637 57.148 40.560 1.00 34.46                        ATOM 2776 O ALA A 365 0 1.906 56.995 39.582 1.00 34.37                        ATOM 2777 CB ALA A 365 0 3.963 55.155 41.301 1.00 33.51                       ATOM 2778 N ASN A 366 0 2.261 57.916 41.571 1.00 34.45                        ATOM 2779 CA ASN A 366 0 1.003 58.619 41.632 1.00 36.37                       ATOM 2780 C ASN A 366 0 0.708 59.524 40.447 1.00 35.60                        ATOM 2781 O ASN A 366 0 -0.462 59.719 40.131 1.00 36.50                       ATOM 2782 CB ASN A 366 0 0.904 59.464 42.918 1.00 38.72                       ATOM 2783 CG ASN A 366 0 0.794 58.558 44.126 1.00 41.08                       ATOM 2784 OD1 ASN A 366 0 0.863 58.966 45.284 1.00 43.39                      ATOM 2785 ND2 ASN A 366 0 0.646 57.256 43.914 1.00 42.72                      ATOM 2786 N ASP A 367 0 1.694 60.046 39.752 1.00 34.06                        ATOM 2787 CA ASP A 367 0 1.571 60.899 38.610 1.00 33.37                       ATOM 2788 C ASP A 367 0 1.566 60.122 37.293 1.00 32.09                        ATOM 2789 O ASP A 367 0 1.430 60.762 36.247 1.00 31.74                        ATOM 2790 CB ASP A 367 0 2.768 61.841 38.483 1.00 35.96                       ATOM 2791 CG ASP A 367 0 3.048 62.818 39.602 1.00 37.69                       ATOM 2792 OD1 ASP A 367 0 2.123 63.209 40.336 1.00 37.23                      ATOM 2793 OD2 ASP A 367 0 4.258 63.194 39.705 1.00 39.62                      ATOM 2794 N LEU A 368 0 1.791 58.814 37.371 1.00 30.39                        ATOM 2795 CA LEU A 368 0 1.897 58.055 36.123 1.00 28.74                       ATOM 2796 C LEU A 368 0 0.586 57.386 35.745 1.00 28.85                        ATOM 2797 O LEU A 368 0 -0.214 56.947 36.555 1.00 28.17                       ATOM 2798 CB LEU A 368 0 3.043 57.046 36.194 1.00 26.94                       ATOM 2799 CG LEU A 368 0 4.436 57.668 36.422 1.00 27.05                       ATOM 2800 CD1 LEU A 368 0 5.455 56.581 36.765 1.00 25.41                      ATOM 2801 CD2 LEU A 368 0 4.882 58.499 35.236 1.00 24.44                      ATOM 2802 N LEU A 369 0 0.392 57.332 34.446 1.00 28.81                        ATOM 2803 CA LEU A 369 0 -0.753 56.671 33.834 1.00 29.65                      ATOM 2804 C LEU A 369 0 -0.238 55.398 33.162 1.00 28.29                       ATOM 2805 O LEU A 369 0 0.875 55.356 32.660 1.00 25.59                        ATOM 2806 CB LEU A 369 0 -1.333 57.668 32.821 1.00 30.27                      ATOM 2807 CG LEU A 369 0 -1.800 58.998 33.456 1.00 32.06                      ATOM 2808 CD1 LEU A 369 0 -2.220 59.979 32.370 1.00 31.87                     ATOM 2809 CD2 LEU A 369 0 -2.932 58.787 34.455 1.00 30.89                     ATOM 2810 N PRO A 370 0 -1.054 54.361 33.157 1.00 27.87                       ATOM 2811 CA PRO A 370 0 -2.396 54.379 33.688 1.00 26.71                      ATOM 2812 C PRO A 370 0 -2.513 54.112 35.169 1.00 26.73                       ATOM 2813 O PRO A 370 0 -1.872 53.184 35.668 1.00 26.55                       ATOM 2814 CB PRO A 370 0 -3.126 53.222 32.958 1.00 27.28                      ATOM 2815 CG PRO A 370 0 -2.003 52.317 32.557 1.00 27.38                      ATOM 2816 CD PRO A 370 0 -0.720 53.102 32.482 1.00 27.24                      ATOM 2817 N ALA A 371 0 -3.414 54.810 35.870 1.00 26.16                       ATOM 2818 CA ALA A 371 0 -3.581 54.556 37.302 1.00 25.73                      ATOM 2819 C ALA A 371 0 -3.892 53.103 37.616 1.00 24.59                       ATOM 2820 O ALA A 371 0 -4.758 52.533 36.946 1.00 25.05                       ATOM 2821 CB ALA A 371 0 -4.718 55.394 37.903 1.00 26.42                      ATOM 2822 N GLY A 372 0 -3.261 52.524 38.625 1.00 22.47                       ATOM 2823 CA GLY A 372 0 -3.519 51.187 39.087 1.00 21.06                      ATOM 2824 C GLY A 372 0 -2.691 50.096 38.427 1.00 23.01                       ATOM 2825 O GLY A 372 0 -2.758 48.928 38.831 1.00 23.85                       ATOM 2826 N SER A 373 0 -1.910 50.428 37.421 1.00 23.30                       ATOM 2827 CA SER A 373 0 -1.054 49.459 36.736 1.00 24.36                      ATOM 2828 C SER A 373 0 0.429 49.746 36.919 1.00 24.76                        ATOM 2829 O SER A 373 0 1.257 49.103 36.270 1.00 25.75                        ATOM 2830 CB SER A 373 0 -1.371 49.584 35.233 1.00 23.25                      ATOM 2831 OG SER A 373 0 -2.638 49.014 34.952 1.00 23.80                      ATOM 2832 N VAL A 374 0 0.779 50.799 37.657 1.00 23.87                        ATOM 2833 CA VAL A 374 0 2.176 51.255 37.706 1.00 22.95                       ATOM 2834 C VAL A 374 0 2.739 51.109 39.105 1.00 21.72                        ATOM 2835 O VAL A 374 0 2.093 51.518 40.059 1.00 21.03                        ATOM 2836 CB VAL A 374 0 2.317 52.687 37.169 1.00 23.05                       ATOM 2837 CG1 VAL A 374 0 3.720 53.273 37.323 1.00 24.13                      ATOM 2838 CG2 VAL A 374 0 1.945 52.771 35.698 1.00 21.58                      ATOM 2839 N TYR A 375 0 3.862 50.402 39.246 1.00 20.52                        ATOM 2840 CA TYR A 375 0 4.445 50.184 40.573 1.00 22.02                       ATOM 2841 C TYR A 375 0 5.873 50.743 40.549 1.00 22.56                        ATOM 2842 O TYR A 375 0 6.665 50.524 39.639 1.00 21.82                        ATOM 2843 CB TYR A 375 0 4.467 48.729 41.067 1.00 21.98                       ATOM 2844 CG TYR A 375 0 3.042 48.217 41.226 1.00 24.04                       ATOM 2845 CD1 TYR A 375 0 2.398 48.261 42.445 1.00 23.57                      ATOM 2846 CD2 TYR A 375 0 2.339 47.760 40.115 1.00 24.92                      ATOM 2847 CE1 TYR A 375 0 1.100 47.831 42.575 1.00 25.65                      ATOM 2848 CE2 TYR A 375 0 1.034 47.327 40.220 1.00 25.89                      ATOM 2849 CZ TYR A 375 0 0.429 47.352 41.464 1.00 26.65                       ATOM 2850 OH TYR A 375 0 -0.869 46.916 41.593 1.00 27.26                      ATOM 2851 N GLU A 376 0 6.130 51.563 41.546 1.00 22.36                        ATOM 2852 CA GLU A 376 0 7.403 52.214 41.718 1.00 23.62                       ATOM 2853 C GLU A 376 0 8.411 51.289 42.387 1.00 22.40                        ATOM 2854 O GLU A 376 0 8.062 50.578 43.324 1.00 21.88                        ATOM 2855 CB GLU A 376 0 7.211 53.465 42.614 1.00 25.13                       ATOM 2856 CG GLU A 376 0 8.500 54.255 42.720 1.00 27.91                       ATOM 2857 CD GLU A 376 0 8.376 55.725 43.046 1.00 29.20                       ATOM 2858 OE1 GLU A 376 0 7.247 56.268 43.109 1.00 30.01                      ATOM 2859 OE2 GLU A 376 0 9.458 56.336 43.219 1.00 28.05                      ATOM 2860 N LEU A 377 0 9.669 51.353 41.954 1.00 21.23                        ATOM 2861 CA LEU A 377 0 10.705 50.535 42.626 1.00 19.95                      ATOM 2862 C LEU A 377 0 11.838 51.478 42.982 1.00 20.30                       ATOM 2863 O LEU A 377 0 12.220 52.350 42.197 1.00 20.12                       ATOM 2864 CB LEU A 377 0 11.129 49.419 41.692 1.00 20.77                      ATOM 2865 CG LEU A 377 0 10.668 47.964 41.818 1.00 20.49                      ATOM 2866 CD1 LEU A 377 0 9.439 47.739 42.629 1.00 17.77                      ATOM 2867 CD2 LEU A 377 0 10.617 47.242 40.483 1.00 19.28                     ATOM 2868 N PRO A 378 0 12.407 51.334 44.162 1.00 19.69                       ATOM 2869 CA PRO A 378 0 13.523 52.117 44.631 1.00 19.91                      ATOM 2870 C PRO A 378 0 14.797 51.650 43.937 1.00 19.81                       ATOM 2871 O PRO A 378 0 14.795 50.645 43.241 1.00 17.74                       ATOM 2872 CB PRO A 378 0 13.611 51.893 46.157 1.00 20.21                      ATOM 2873 CG PRO A 378 0 12.957 50.546 46.291 1.00 20.73                      ATOM 2874 CD PRO A 378 0 12.050 50.292 45.114 1.00 19.74                      ATOM 2875 N ARG A 379 0 15.877 52.410 44.059 1.00 19.68                       ATOM 2876 CA ARG A 379 0 17.172 52.135 43.449 1.00 18.58                      ATOM 2877 C ARG A 379 0 18.027 51.129 44.193 1.00 18.68                       ATOM 2878 O ARG A 379 0 18.151 51.126 45.432 1.00 17.60                       ATOM 2879 CB ARG A 379 0 17.946 53.487 43.431 1.00 18.33                      ATOM 2880 CG ARG A 379 0 19.406 53.348 43.030 1.00 19.33                      ATOM 2881 CD ARG A 379 0 20.026 54.710 42.729 1.00 19.06                      ATOM 2882 NE ARG A 379 0 21.413 54.561 42.295 1.00 16.65                      ATOM 2883 CZ ARG A 379 0 21.794 54.681 41.031 1.00 15.60                      ATOM 2884 NH1 ARG A 379 0 20.964 54.904 40.038 1.00 14.29                     ATOM 2885 NH2 ARG A 379 0 23.096 54.505 40.783 1.00 17.29                     ATOM 2886 N ASN A 380 0 18.701 50.263 43.441 1.00 20.11                       ATOM 2887 CA ASN A 380 0 19.658 49.328 44.011 1.00 21.97                      ATOM 2888 C ASN A 380 0 19.129 48.604 45.227 1.00 22.44                       ATOM 2889 O ASN A 380 0 19.712 48.630 46.317 1.00 22.53                       ATOM 2890 CB ASN A 380 0 20.995 50.045 44.345 1.00 23.30                      ATOM 2891 CG ASN A 380 0 21.860 50.231 43.107 1.00 25.83                      ATOM 2892 OD1 ASN A 380 0 22.636 51.186 42.877 1.00 27.14                     ATOM 2893 ND2 ASN A 380 0 21.767 49.271 42.185 1.00 24.91                     ATOM 2894 N GLN A 381 0 17.974 47.936 45.097 1.00 21.39                       ATOM 2895 CA GLN A 381 0 17.468 47.162 46.220 1.00 20.88                      ATOM 2896 C GLN A 381 0 17.169 45.760 45.679 1.00 19.96                       ATOM 2897 O GLN A 381 0 17.000 45.635 44.471 1.00 19.90                       ATOM 2898 CB GLN A 381 0 16.219 47.722 46.871 1.00 22.84                      ATOM 2899 CG GLN A 381 0 16.326 49.172 47.318 1.00 27.28                      ATOM 2900 CD GLN A 381 0 16.065 49.297 48.792 1.00 30.24                      ATOM 2901 OE1 GLN A 381 0 15.067 49.917 49.171 1.00 34.48                     ATOM 2902 NE2 GLN A 381 0 16.929 48.742 49.611 1.00 30.80                     ATOM 2903 N VAL A 382 0 17.046 44.825 46.594 1.00 18.67                       ATOM 2904 CA VAL A 382 0 16.665 43.472 46.248 1.00 18.98                      ATOM 2905 C VAL A 382 0 15.139 43.327 46.212 1.00 19.75                       ATOM 2906 O VAL A 382 0 14.443 43.550 47.225 1.00 18.76                       ATOM 2907 CB VAL A 382 0 17.252 42.491 47.278 1.00 19.03                      ATOM 2908 CG1 VAL A 382 0 16.811 41.065 46.960 1.00 18.87                     ATOM 2909 CG2 VAL A 382 0 18.779 42.637 47.344 1.00 17.54                     ATOM 2910 N VAL A 383 0 14.601 42.954 45.046 1.00 17.58                       ATOM 2911 CA VAL A 383 0 13.151 42.715 45.037 1.00 17.76                      ATOM 2912 C VAL A 383 0 12.777 41.254 44.883 1.00 17.50                       ATOM 2913 O VAL A 383 0 13.348 40.472 44.153 1.00 16.42                       ATOM 2914 CB VAL A 383 0 12.306 43.626 44.145 1.00 17.69                      ATOM 2915 CG1 VAL A 383 0 13.111 44.759 43.585 1.00 15.33                     ATOM 2916 CG2 VAL A 383 0 11.400 43.009 43.126 1.00 17.79                     ATOM 2917 N GLU A 384 0 11.743 40.861 45.638 1.00 18.47                       ATOM 2918 CA GLU A 384 0 11.173 39.529 45.542 1.00 18.27                      ATOM 2919 C GLU A 384 0 9.711 39.683 45.096 1.00 18.94                        ATOM 2920 O GLU A 384 0 8.956 40.311 45.816 1.00 19.06                        ATOM 2921 CB GLU A 384 0 11.253 38.764 46.852 1.00 17.12                      ATOM 2922 CG GLU A 384 0 10.717 37.345 46.738 1.00 17.52                      ATOM 2923 CD GLU A 384 0 10.979 36.551 47.998 1.00 19.10                      ATOM 2924 OE1 GLU A 384 0 12.101 36.050 48.218 1.00 20.69                     ATOM 2925 OE2 GLU A 384 0 10.018 36.405 48.773 1.00 21.22                     ATOM 2926 N LEU A 385 0 9.326 39.182 43.948 1.00 19.78                        ATOM 2927 CA LEU A 385 0 7.966 39.153 43.463 1.00 21.07                       ATOM 2928 C LEU A 385 0 7.391 37.738 43.591 1.00 20.91                        ATOM 2929 O LEU A 385 0 8.043 36.790 43.113 1.00 21.40                        ATOM 2930 CB LEU A 385 0 7.881 39.466 41.959 1.00 20.92                       ATOM 2931 CG LEU A 385 0 8.393 40.795 41.457 1.00 23.75                       ATOM 2932 CD1 LEU A 385 0 8.118 40.984 39.962 1.00 23.01                      ATOM 2933 CD2 LEU A 385 0 7.827 41.977 42.244 1.00 22.40                      ATOM 2934 N VAL A 386 0 6.182 37.574 44.099 1.00 20.91                        ATOM 2935 CA VAL A 386 0 5.510 36.274 44.189 1.00 19.03                       ATOM 2936 C VAL A 386 0 4.228 36.334 43.356 1.00 21.11                        ATOM 2937 O VAL A 386 0 3.465 37.326 43.516 1.00 20.56                        ATOM 2938 CB VAL A 386 0 5.159 35.967 45.654 1.00 20.91                       ATOM 2939 CG1 VAL A 386 0 4.518 34.575 45.739 1.00 20.40                      ATOM 2940 CG2 VAL A 386 0 6.321 36.044 46.625 1.00 19.89                      ATOM 2941 N VAL A 387 0 4.011 35.469 42.358 1.00 20.02                        ATOM 2942 CA VAL A 387 0 2.817 35.515 41.491 1.00 20.83                       ATOM 2943 C VAL A 387 0 2.119 34.152 41.385 1.00 21.15                        ATOM 2944 O VAL A 387 0 2.369 33.285 40.528 1.00 19.97                        ATOM 2945 CB VAL A 387 0 3.163 36.076 40.104 1.00 20.91                       ATOM 2946 CG1 VAL A 387 0 1.917 36.472 39.297 1.00 22.49                      ATOM 2947 CG2 VAL A 387 0 3.959 37.393 40.171 1.00 22.24                      ATOM 2948 N PRO A 388 0 1.262 33.832 42.358 1.00 20.55                        ATOM 2949 CA PRO A 388 0 0.570 32.548 42.483 1.00 20.93                       ATOM 2950 C PRO A 388 0 -0.271 32.226 41.264 1.00 20.76                       ATOM 2951 O PRO A 388 0 -0.928 33.118 40.715 1.00 19.53                       ATOM 2952 CB PRO A 388 0 -0.310 32.559 43.757 1.00 20.54                      ATOM 2953 CG PRO A 388 0 0.280 33.766 44.482 1.00 21.86                       ATOM 2954 CD PRO A 388 0 0.841 34.707 43.438 1.00 20.83                       ATOM 2955 N ALA A 389 0 -0.160 30.986 40.807 1.00 21.68                       ATOM 2956 CA ALA A 389 0 -0.983 30.617 39.640 1.00 24.20                      ATOM 2957 C ALA A 389 0 -2.394 30.320 40.148 1.00 25.02                       ATOM 2958 O ALA A 389 0 -2.619 30.162 41.350 1.00 24.19                       ATOM 2959 CB ALA A 389 0 -0.383 29.403 38.968 1.00 23.67                      ATOM 2960 N GLY A 390 0 -3.309 30.143 39.222 1.00 28.43                       ATOM 2961 CA GLY A 390 0 -4.713 29.811 39.539 1.00 28.47                      ATOM 2962 C GLY A 390 0 -5.624 30.325 38.431 1.00 28.63                       ATOM 2963 O GLY A 390 0 -6.512 29.630 37.937 1.00 31.26                       ATOM 2964 N VAL A 391 0 -5.402 31.531 37.961 1.00 27.11                       ATOM 2965 CA VAL A 391 0 -6.234 32.164 36.962 1.00 26.51                      ATOM 2966 C VAL A 391 0 -6.246 31.377 35.666 1.00 29.59                       ATOM 2967 O VAL A 391 0 -5.274 30.775 35.181 1.00 30.61                       ATOM 2968 CB VAL A 391 0 -5.835 33.634 36.788 1.00 25.83                      ATOM 2969 CG1 VAL A 391 0 -4.584 33.787 35.937 1.00 24.18                     ATOM 2970 CG2 VAL A 391 0 -7.017 34.419 36.219 1.00 24.11                     ATOM 2971 N LEU A 392 0 -7.439 31.392 35.058 1.00 30.83                       ATOM 2972 CA LEU A 392 0 -7.705 30.604 33.867 1.00 30.29                      ATOM 2973 C LEU A 392 0 -6.809 31.004 32.710 1.00 27.38                       ATOM 2974 O LEU A 392 0 -6.316 32.113 32.665 1.00 24.62                       ATOM 2975 CB LEU A 392 0 -9.173 30.726 33.436 1.00 32.58                      ATOM 2976 CG LEU A 392 0 -9.711 32.126 33.189 1.00 33.97                      ATOM 2977 CD1 LEU A 392 0 -9.411 32.626 31.786 1.00 34.78                     ATOM 2978 CD2 LEU A 392 0 -11.225 32.122 33.463 1.00 36.03                    ATOM 2979 N GLY A 393 0 -6.725 30.074 31.754 1.00 26.24                       ATOM 2980 CA GLY A 393 0 -5.936 30.302 30.554 1.00 25.54                      ATOM 2981 C GLY A 393 0 -4.458 29.994 30.710 1.00 25.81                       ATOM 2982 O GLY A 393 0 -3.686 30.361 29.820 1.00 26.67                       ATOM 2983 N GLY A 394 0 -4.033 29.379 31.803 1.00 25.84                       ATOM 2984 CA GLY A 394 0 -2.615 29.112 32.035 1.00 25.94                      ATOM 2985 C GLY A 394 0 -2.140 27.844 31.348 1.00 26.00                       ATOM 2986 O GLY A 394 0 -2.884 27.193 30.625 1.00 25.18                       ATOM 2987 N PRO A 395 0 -0.860 27.527 31.517 1.00 24.26                       ATOM 2988 CA PRO A 395 0 0.051 28.258 32.364 1.00 21.79                       ATOM 2989 C PRO A 395 0 0.517 29.518 31.660 1.00 19.29                        ATOM 2990 O PRO A 395 0 0.704 29.597 30.445 1.00 17.41                        ATOM 2991 CB PRO A 395 0 1.159 27.279 32.794 1.00 22.52                       ATOM 2992 CG PRO A 395 0 1.062 26.223 31.758 1.00 24.35                       ATOM 2993 CD PRO A 395 0 -0.241 26.312 30.973 1.00 24.87                      ATOM 2994 N HIS A 396 0 0.586 30.591 32.451 1.00 16.97                        ATOM 2995 CA HIS A 396 0 0.970 31.917 31.980 1.00 15.05                       ATOM 2996 C HIS A 396 0 2.477 32.137 32.186 1.00 15.41                        ATOM 2997 O HIS A 396 0 3.039 32.025 33.275 1.00 14.21                        ATOM 2998 CB HIS A 396 0 0.288 32.989 32.842 1.00 15.40                       ATOM 2999 CG HIS A 396 0 -1.224 32.924 32.737 1.00 18.23                      ATOM 3000 ND1 HIS A 396 0 -1.942 33.504 31.702 1.00 16.23                     ATOM 3001 CD2 HIS A 396 0 -2.109 32.319 33.557 1.00 17.00                     ATOM 3002 CE1 HIS A 396 0 -3.218 33.262 31.906 1.00 18.22                     ATOM 3003 NE2 HIS A 396 0 -3.343 32.526 33.014 1.00 19.08                     ATOM 3004 N PRO A 397 0 3.143 32.403 31.090 1.00 14.69                        ATOM 3005 CA PRO A 397 0 4.593 32.617 31.080 1.00 16.91                       ATOM 3006 C PRO A 397 0 4.818 34.129 31.202 1.00 17.59                        ATOM 3007 O PRO A 397 0 4.524 34.843 30.235 1.00 17.59                        ATOM 3008 CB PRO A 397 0 5.076 32.040 29.757 1.00 16.63                       ATOM 3009 CG PRO A 397 0 3.785 31.844 28.978 1.00 17.83                       ATOM 3010 CD PRO A 397 0 2.620 32.464 29.736 1.00 14.36                       ATOM 3011 N PHE A 398 0 5.242 34.590 32.377 1.00 16.39                        ATOM 3012 CA PHE A 398 0 5.462 36.019 32.529 1.00 15.95                       ATOM 3013 C PHE A 398 0 6.906 36.365 32.168 1.00 15.74                        ATOM 3014 O PHE A 398 0 7.846 35.619 32.444 1.00 15.78                        ATOM 3015 CB PHE A 398 0 5.173 36.455 33.963 1.00 17.20                       ATOM 3016 CG PHE A 398 0 3.817 37.073 34.169 1.00 19.23                       ATOM 3017 CD1 PHE A 398 0 2.673 36.299 34.005 1.00 19.58                      ATOM 3018 CD2 PHE A 398 0 3.688 38.403 34.537 1.00 19.42                      ATOM 3019 CE1 PHE A 398 0 1.409 36.832 34.198 1.00 19.83                      ATOM 3020 CE2 PHE A 398 0 2.405 38.933 34.709 1.00 21.46                      ATOM 3021 CZ PHE A 398 0 1.260 38.162 34.539 1.00 19.65                       ATOM 3022 N HIS A 399 0 7.080 37.562 31.640 1.00 14.77                        ATOM 3023 CA HIS A 399 0 8.374 38.089 31.333 1.00 14.75                       ATOM 3024 C HIS A 399 0 8.580 39.496 31.872 1.00 17.67                        ATOM 3025 O HIS A 399 0 7.635 40.308 31.925 1.00 18.29                        ATOM 3026 CB HIS A 399 0 8.582 37.968 29.861 1.00 14.01                       ATOM 3027 CG HIS A 399 0 8.747 39.105 28.962 1.00 16.26                       ATOM 3028 ND1 HIS A 399 0 9.957 39.511 28.446 1.00 15.35                      ATOM 3029 CD2 HIS A 399 0 7.788 39.903 28.386 1.00 17.58                      ATOM 3030 CE1 HIS A 399 0 9.764 40.507 27.593 1.00 15.61                      ATOM 3031 NE2 HIS A 399 0 8.457 40.770 27.548 1.00 17.52                      ATOM 3032 N LEU A 400 0 9.837 39.771 32.201 1.00 15.57                        ATOM 3033 CA LEU A 400 0 10.220 41.061 32.745 1.00 16.93                      ATOM 3034 C LEU A 400 0 11.207 41.732 31.788 1.00 16.51                       ATOM 3035 O LEU A 400 0 12.268 41.175 31.510 1.00 15.77                       ATOM 3036 CB LEU A 400 0 10.913 40.825 34.084 1.00 18.17                      ATOM 3037 CG LEU A 400 0 10.877 41.741 35.288 1.00 21.27                      ATOM 3038 CD1 LEU A 400 0 12.130 41.638 36.151 1.00 19.27                     ATOM 3039 CD2 LEU A 400 0 10.536 43.166 34.926 1.00 19.86                     ATOM 3040 N HIS A 401 0 10.945 42.916 31.321 1.00 14.34                       ATOM 3041 CA HIS A 401 0 11.830 43.707 30.506 1.00 16.06                      ATOM 3042 C HIS A 401 0 12.924 44.300 31.428 1.00 16.15                       ATOM 3043 O HIS A 401 0 12.644 44.543 32.600 1.00 13.61                       ATOM 3044 CB HIS A 401 0 11.105 44.884 29.843 1.00 13.27                      ATOM 3045 CG HIS A 401 0 10.184 44.441 28.751 1.00 14.50                      ATOM 3046 ND1 HIS A 401 0 10.201 44.973 27.479 1.00 14.96                     ATOM 3047 CD2 HIS A 401 0 9.202 43.492 28.750 1.00 12.35                      ATOM 3048 CE1 HIS A 401 0 9.263 44.387 26.725 1.00 12.61                      ATOM 3049 NE2 HIS A 401 0 8.677 43.507 27.492 1.00 12.41                      ATOM 3050 N GLY A 402 0 14.103 44.549 30.855 1.00 15.59                       ATOM 3051 CA GLY A 402 0 15.152 45.209 31.598 1.00 15.18                      ATOM 3052 C GLY A 402 0 16.009 44.351 32.510 1.00 15.96                       ATOM 3053 O GLY A 402 0 16.927 44.898 33.170 1.00 16.30                       ATOM 3054 N HIS A 403 0 15.618 43.147 32.893 1.00 12.96                       ATOM 3055 CA HIS A 403 0 16.282 42.337 33.873 1.00 15.00                      ATOM 3056 C HIS A 403 0 16.226 40.839 33.586 1.00 15.22                       ATOM 3057 O HIS A 403 0 15.253 40.381 32.971 1.00 16.16                       ATOM 3058 CB HIS A 403 0 15.525 42.478 35.227 1.00 14.13                      ATOM 3059 CG HIS A 403 0 15.571 43.829 35.827 1.00 16.69                      ATOM 3060 ND1 HIS A 403 0 16.604 44.253 36.649 1.00 16.13                     ATOM 3061 CD2 HIS A 403 0 14.744 44.911 35.659 1.00 15.50                     ATOM 3062 CE1 HIS A 403 0 16.425 45.520 37.002 1.00 15.02                     ATOM 3063 NE2 HIS A 403 0 15.285 45.905 36.430 1.00 16.15                     ATOM 3064 N ALA A 404 0 17.138 40.054 34.113 1.00 13.71                       ATOM 3065 CA ALA A 404 0 17.039 38.607 34.158 1.00 12.60                      ATOM 3066 C ALA A 404 0 16.771 38.370 35.649 1.00 12.31                       ATOM 3067 O ALA A 404 0 17.156 39.291 36.373 1.00 13.94                       ATOM 3068 CB ALA A 404 0 18.249 37.819 33.721 1.00 13.84                      ATOM 3069 N PHE A 405 0 16.085 37.356 36.126 1.00 12.21                       ATOM 3070 CA PHE A 405 0 15.813 37.235 37.559 1.00 11.64                      ATOM 3071 C PHE A 405 0 16.177 35.821 38.008 1.00 12.55                       ATOM 3072 O PHE A 405 0 16.196 34.883 37.201 1.00 12.23                       ATOM 3073 CB PHE A 405 0 14.325 37.487 37.907 1.00 11.82                      ATOM 3074 CG PHE A 405 0 13.382 36.893 36.879 1.00 11.75                      ATOM 3075 CD1 PHE A 405 0 13.030 35.557 36.933 1.00 10.76                     ATOM 3076 CD2 PHE A 405 0 12.917 37.663 35.824 1.00 11.55                     ATOM 3077 CE1 PHE A 405 0 12.189 35.002 35.978 1.00 11.52                     ATOM 3078 CE2 PHE A 405 0 12.087 37.112 34.862 1.00 13.32                     ATOM 3079 CZ PHE A 405 0 11.692 35.767 34.946 1.00 11.45                      ATOM 3080 N SER A 406 0 16.414 35.625 39.288 1.00 12.86                       ATOM 3081 CA SER A 406 0 16.660 34.286 39.796 1.00 13.43                      ATOM 3082 C SER A 406 0 15.276 33.712 40.130 1.00 13.49                       ATOM 3083 O SER A 406 0 14.518 34.375 40.847 1.00 10.13                       ATOM 3084 CB SER A 406 0 17.433 34.290 41.123 1.00 13.78                      ATOM 3085 OG SER A 406 0 18.708 34.834 40.938 1.00 16.72                      ATOM 3086 N VAL A 407 0 15.100 32.453 39.741 1.00 14.53                       ATOM 3087 CA VAL A 407 0 13.853 31.777 40.093 1.00 13.90                      ATOM 3088 C VAL A 407 0 14.160 30.943 41.325 1.00 14.53                       ATOM 3089 O VAL A 407 0 14.513 29.753 41.262 1.00 14.62                       ATOM 3090 CB VAL A 407 0 13.333 30.903 38.941 1.00 16.43                      ATOM 3091 CG1 VAL A 407 0 11.969 30.317 39.341 1.00 16.69                     ATOM 3092 CG2 VAL A 407 0 13.272 31.682 37.626 1.00 14.90                     ATOM 3093 N VAL A 408 0 13.971 31.544 42.485 1.00 14.32                       ATOM 3094 CA VAL A 408 0 14.173 30.947 43.780 1.00 15.47                      ATOM 3095 C VAL A 408 0 13.115 29.870 44.049 1.00 16.51                       ATOM 3096 O VAL A 408 0 13.387 28.927 44.812 1.00 17.39                       ATOM 3097 CB VAL A 408 0 14.280 31.967 44.932 1.00 15.75                      ATOM 3098 CG1 VAL A 408 0 15.345 33.015 44.600 1.00 14.81                     ATOM 3099 CG2 VAL A 408 0 12.952 32.693 45.189 1.00 15.99                     ATOM 3100 N ARG A 409 0 11.972 29.940 43.387 1.00 16.28                       ATOM 3101 CA ARG A 409 0 10.960 28.900 43.570 1.00 17.67                      ATOM 3102 C ARG A 409 0 10.217 28.757 42.236 1.00 17.09                       ATOM 3103 O ARG A 409 0 9.585 29.698 41.763 1.00 15.25                        ATOM 3104 CB ARG A 409 0 9.993 29.143 44.718 1.00 17.87                       ATOM 3105 CG ARG A 409 0 8.796 28.188 44.663 1.00 21.12                       ATOM 3106 CD ARG A 409 0 8.008 28.181 45.945 1.00 22.10                       ATOM 3107 NE ARG A 409 0 6.801 27.370 45.955 1.00 24.80                       ATOM 3108 CZ ARG A 409 0 5.918 27.361 46.961 1.00 25.93                       ATOM 3109 NH1 ARG A 409 0 4.859 26.569 46.877 1.00 27.14                      ATOM 3110 NH2 ARG A 409 0 6.068 28.117 48.046 1.00 25.44                      ATOM 3111 N SER A 410 0 10.366 27.576 41.668 1.00 16.33                       ATOM 3112 CA SER A 410 0 9.802 27.245 40.373 1.00 18.33                       ATOM 3113 C SER A 410 0 8.406 26.612 40.492 1.00 18.60                        ATOM 3114 O SER A 410 0 7.941 26.223 41.566 1.00 16.94                        ATOM 3115 CB SER A 410 0 10.724 26.199 39.705 1.00 19.51                      ATOM 3116 OG SER A 410 0 11.718 26.865 38.933 1.00 20.28                      ATOM 3117 N ALA A 411 0 7.754 26.551 39.343 1.00 18.19                        ATOM 3118 CA ALA A 411 0 6.458 25.899 39.231 1.00 19.76                       ATOM 3119 C ALA A 411 0 6.667 24.406 39.474 1.00 22.62                        ATOM 3120 O ALA A 411 0 7.636 23.759 39.067 1.00 20.97                        ATOM 3121 CB ALA A 411 0 5.873 26.075 37.841 1.00 17.13                       ATOM 3122 N GLY A 412 0 5.710 23.856 40.229 1.00 26.30                        ATOM 3123 CA GLY A 412 0 5.714 22.442 40.558 1.00 27.05                       ATOM 3124 C GLY A 412 0 6.692 22.150 41.677 1.00 29.22                        ATOM 3125 O GLY A 412 0 6.917 20.959 41.944 1.00 32.10                        ATOM 3126 N SER A 413 0 7.293 23.139 42.322 1.00 28.66                        ATOM 3127 CA SER A 413 0 8.223 22.871 43.400 1.00 28.58                       ATOM 3128 C SER A 413 0 7.757 23.600 44.642 1.00 29.64                        ATOM 3129 O SER A 413 0 7.279 24.735 44.524 1.00 30.66                        ATOM 3130 CB SER A 413 0 9.610 23.407 43.015 1.00 30.12                       ATOM 3131 OG SER A 413 0 10.484 23.233 44.127 1.00 31.74                      ATOM 3132 N SER A 414 0 7.902 23.031 45.819 1.00 29.19                        ATOM 3133 CA SER A 414 0 7.523 23.753 47.033 1.00 30.71                       ATOM 3134 C SER A 414 0 8.762 24.124 47.834 1.00 30.51                        ATOM 3135 O SER A 414 0 8.746 24.453 49.017 1.00 31.90                        ATOM 3136 CB SER A 414 0 6.612 22.832 47.853 1.00 31.10                       ATOM 3137 OG SER A 414 0 7.438 21.764 48.299 1.00 34.24                       ATOM 3138 N THR A 415 0 9.919 24.063 47.194 1.00 30.60                        ATOM 3139 CA THR A 415 0 11.194 24.336 47.860 1.00 30.60                      ATOM 3140 C THR A 415 0 11.819 25.614 47.291 1.00 27.71                       ATOM 3141 O THR A 415 0 11.582 25.998 46.137 1.00 27.49                       ATOM 3142 CB THR A 415 0 12.089 23.095 47.747 1.00 32.16                      ATOM 3143 OG1 THR A 415 0 13.411 23.441 47.285 1.00 35.60                     ATOM 3144 CG2 THR A 415 0 11.599 22.103 46.710 1.00 34.11                     ATOM 3145 N TYR A 416 0 12.662 26.268 48.053 1.00 24.34                       ATOM 3146 CA TYR A 416 0 13.288 27.513 47.621 1.00 25.69                      ATOM 3147 C TYR A 416 0 14.782 27.297 47.392 1.00 24.69                       ATOM 3148 O TYR A 416 0 15.364 26.603 48.211 1.00 25.96                       ATOM 3149 CB TYR A 416 0 13.129 28.633 48.659 1.00 23.79                      ATOM 3150 CG TYR A 416 0 11.690 29.091 48.794 1.00 24.53                      ATOM 3151 CD1 TYR A 416 0 10.789 28.387 49.596 1.00 24.14                     ATOM 3152 CD2 TYR A 416 0 11.230 30.219 48.131 1.00 23.99                     ATOM 3153 CE1 TYR A 416 0 9.474 28.799 49.713 1.00 23.70                      ATOM 3154 CE2 TYR A 416 0 9.922 30.641 48.248 1.00 23.96                      ATOM 3155 CZ TYR A 416 0 9.050 29.929 49.054 1.00 23.73                       ATOM 3156 OH TYR A 416 0 7.744 30.337 49.152 1.00 23.53                       ATOM 3157 N ASN A 417 0 15.360 27.867 46.353 1.00 22.34                       ATOM 3158 CA ASN A 417 0 16.810 27.702 46.223 1.00 20.83                      ATOM 3159 C ASN A 417 0 17.425 29.089 46.092 1.00 20.43                       ATOM 3160 O ASN A 417 0 17.247 29.761 45.082 1.00 20.00                       ATOM 3161 CB ASN A 417 0 17.179 26.763 45.086 1.00 19.72                      ATOM 3162 CG ASN A 417 0 18.660 26.716 44.758 1.00 19.50                      ATOM 3163 OD1 ASN A 417 0 19.485 27.313 45.465 1.00 20.18                     ATOM 3164 ND2 ASN A 417 0 18.981 26.043 43.660 1.00 17.21                     ATOM 3165 N PHE A 418 0 18.153 29.508 47.119 1.00 20.79                       ATOM 3166 CA PHE A 418 0 18.831 30.797 47.049 1.00 20.77                      ATOM 3167 C PHE A 418 0 20.314 30.613 46.725 1.00 20.47                       ATOM 3168 O PHE A 418 0 20.973 31.618 46.517 1.00 19.47                       ATOM 3169 CB PHE A 418 0 18.764 31.542 48.384 1.00 20.52                      ATOM 3170 CG PHE A 418 0 17.332 31.821 48.753 1.00 22.19                      ATOM 3171 CD1 PHE A 418 0 16.644 30.947 49.578 1.00 21.36                     ATOM 3172 CD2 PHE A 418 0 16.697 32.951 48.244 1.00 21.95                     ATOM 3173 CE1 PHE A 418 0 15.320 31.208 49.919 1.00 21.64                     ATOM 3174 CE2 PHE A 418 0 15.386 33.198 48.599 1.00 22.81                     ATOM 3175 CZ PHE A 418 0 14.694 32.325 49.419 1.00 22.57                      ATOM 3176 N VAL A 419 0 20.816 29.380 46.732 1.00 19.72                       ATOM 3177 CA VAL A 419 0 22.272 29.235 46.564 1.00 19.96                      ATOM 3178 C VAL A 419 0 22.682 29.261 45.114 1.00 20.65                       ATOM 3179 O VAL A 419 0 23.634 29.875 44.671 1.00 21.02                       ATOM 3180 CB VAL A 419 0 22.708 27.888 47.200 1.00 21.81                      ATOM 3181 CG1 VAL A 419 0 23.954 27.291 46.588 1.00 21.97                     ATOM 3182 CG2 VAL A 419 0 22.885 28.098 48.713 1.00 21.55                     ATOM 3183 N ASN A 420 0 21.867 28.585 44.327 1.00 19.77                       ATOM 3184 CA ASN A 420 0 22.076 28.232 42.967 1.00 21.81                      ATOM 3185 C ASN A 420 0 21.028 28.263 41.891 1.00 20.21                       ATOM 3186 O ASN A 420 0 21.046 27.407 41.004 1.00 20.13                       ATOM 3187 CB ASN A 420 0 22.166 26.587 43.207 1.00 21.91                      ATOM 3188 CG ASN A 420 0 23.441 26.231 42.529 1.00 24.12                      ATOM 3189 OD1 ASN A 420 0 23.933 25.113 42.403 1.00 26.75                     ATOM 3190 ND2 ASN A 420 0 24.051 27.318 42.027 1.00 25.42                     ATOM 3191 N PRO A 421 0 19.987 29.034 42.038 1.00 20.27                       ATOM 3192 CA PRO A 421 0 18.808 28.951 41.183 1.00 17.57                      ATOM 3193 C PRO A 421 0 19.100 29.369 39.778 1.00 15.76                       ATOM 3194 O PRO A 421 0 19.907 30.281 39.586 1.00 15.13                       ATOM 3195 CB PRO A 421 0 17.769 29.850 41.894 1.00 19.52                      ATOM 3196 CG PRO A 421 0 18.674 30.863 42.589 1.00 19.88                      ATOM 3197 CD PRO A 421 0 19.847 30.057 43.095 1.00 20.45                      ATOM 3198 N VAL A 422 0 18.385 28.803 38.820 1.00 15.28                       ATOM 3199 CA VAL A 422 0 18.502 29.239 37.420 1.00 13.48                      ATOM 3200 C VAL A 422 0 18.157 30.721 37.397 1.00 14.53                       ATOM 3201 O VAL A 422 0 17.340 31.208 38.183 1.00 14.44                       ATOM 3202 CB VAL A 422 0 17.498 28.435 36.585 1.00 15.23                      ATOM 3203 CG1 VAL A 422 0 16.032 28.747 36.937 1.00 13.85                     ATOM 3204 CG2 VAL A 422 0 17.681 28.514 35.089 1.00 13.26                     ATOM 3205 N LYS A 423 0 18.691 31.447 36.451 1.00 15.35                       ATOM 3206 CA LYS A 423 0 18.366 32.831 36.189 1.00 17.23                      ATOM 3207 C LYS A 423 0 17.759 32.891 34.784 1.00 16.55                       ATOM 3208 O LYS A 423 0 18.284 32.189 33.909 1.00 16.92                       ATOM 3209 CB LYS A 423 0 19.627 33.681 36.174 1.00 19.33                      ATOM 3210 CG LYS A 423 0 20.118 33.985 37.565 1.00 24.09                      ATOM 3211 CD LYS A 423 0 21.065 35.206 37.466 1.00 27.32                      ATOM 3212 CE LYS A 423 0 22.470 34.596 37.263 1.00 28.78                      ATOM 3213 NZ LYS A 423 0 23.128 34.482 38.595 1.00 29.50                      ATOM 3214 N ARG A 424 0 16.630 33.570 34.617 1.00 15.85                       ATOM 3215 CA ARG A 424 0 16.016 33.592 33.294 1.00 16.20                      ATOM 3216 C ARG A 424 0 15.235 34.890 33.105 1.00 14.86                       ATOM 3217 O ARG A 424 0 15.354 35.771 33.959 1.00 14.64                       ATOM 3218 CB ARG A 424 0 15.158 32.367 32.994 1.00 16.11                      ATOM 3219 CG ARG A 424 0 14.036 31.864 33.849 1.00 14.06                      ATOM 3220 CD ARG A 424 0 13.447 30.506 33.427 1.00 11.65                      ATOM 3221 NE ARG A 424 0 13.422 30.395 31.961 1.00 9.03                       ATOM 3222 CZ ARG A 424 0 13.312 29.234 31.319 1.00 10.63                      ATOM 3223 NH1 ARG A 424 0 13.185 28.133 32.082 1.00 11.02                     ATOM 3224 NH2 ARG A 424 0 13.403 29.213 29.988 1.00 8.52                      ATOM 3225 N ASP A 425 0 14.519 34.975 31.995 1.00 13.83                       ATOM 3226 CA ASP A 425 0 13.751 36.209 31.752 1.00 15.00                      ATOM 3227 C ASP A 425 0 12.298 35.929 31.359 1.00 15.65                       ATOM 3228 O ASP A 425 0 11.474 36.850 31.271 1.00 15.11                       ATOM 3229 CB ASP A 425 0 14.499 37.130 30.797 1.00 12.96                      ATOM 3230 CG ASP A 425 0 14.609 36.652 29.371 1.00 14.32                      ATOM 3231 OD1 ASP A 425 0 13.697 35.957 28.818 1.00 13.30                     ATOM 3232 OD2 ASP A 425 0 15.632 37.003 28.729 1.00 13.76                     ATOM 3233 N VAL A 426 0 11.883 34.675 31.206 1.00 15.21                       ATOM 3234 CA VAL A 426 0 10.530 34.229 30.984 1.00 13.92                      ATOM 3235 C VAL A 426 0 10.247 33.000 31.865 1.00 13.98                       ATOM 3236 O VAL A 426 0 10.891 31.965 31.696 1.00 15.56                       ATOM 3237 CB VAL A 426 0 10.128 33.807 29.567 1.00 12.49                      ATOM 3238 CG1 VAL A 426 0 8.629 33.473 29.531 1.00 13.99                      ATOM 3239 CG2 VAL A 426 0 10.390 34.874 28.536 1.00 12.37                     ATOM 3240 N VAL A 427 0 9.274 33.090 32.766 1.00 12.82                        ATOM 3241 CA VAL A 427 0 8.979 31.969 33.639 1.00 12.27                       ATOM 3242 C VAL A 427 0 7.495 31.589 33.651 1.00 14.14                        ATOM 3243 O VAL A 427 0 6.594 32.426 33.682 1.00 14.10                        ATOM 3244 CB VAL A 427 0 9.458 32.315 35.056 1.00 11.46                       ATOM 3245 CG1 VAL A 427 0 8.732 33.549 35.594 1.00 9.39                       ATOM 3246 CG2 VAL A 427 0 9.353 31.116 35.982 1.00 10.53                      ATOM 3247 N SER A 428 0 7.229 30.282 33.622 1.00 13.74                        ATOM 3248 CA SER A 428 0 5.889 29.766 33.721 1.00 15.16                       ATOM 3249 C SER A 428 0 5.445 29.878 35.171 1.00 15.48                        ATOM 3250 O SER A 428 0 6.186 29.505 36.087 1.00 15.38                        ATOM 3251 CB SER A 428 0 5.776 28.323 33.206 1.00 16.37                       ATOM 3252 OG SER A 428 0 4.464 27.821 33.484 1.00 17.00                       ATOM 3253 N LEU A 429 0 4.246 30.376 35.399 1.00 15.74                        ATOM 3254 CA LEU A 429 0 3.686 30.489 36.744 1.00 15.73                       ATOM 3255 C LEU A 429 0 3.035 29.184 37.198 1.00 16.41                        ATOM 3256 O LEU A 429 0 2.741 29.041 38.390 1.00 15.74                        ATOM 3257 CB LEU A 429 0 2.669 31.627 36.886 1.00 14.99                       ATOM 3258 CG LEU A 429 0 3.155 33.027 36.540 1.00 16.60                       ATOM 3259 CD1 LEU A 429 0 2.043 34.042 36.862 1.00 17.78                      ATOM 3260 CD2 LEU A 429 0 4.438 33.386 37.281 1.00 16.26                      ATOM 3261 N GLY A 430 0 2.913 28.218 36.295 1.00 17.70                        ATOM 3262 CA GLY A 430 0 2.419 26.904 36.701 1.00 19.84                       ATOM 3263 C GLY A 430 0 0.894 26.836 36.778 1.00 20.72                        ATOM 3264 O GLY A 430 0 0.178 27.498 36.029 1.00 20.89                        ATOM 3265 N VAL A 431 0 0.428 26.056 37.729 1.00 22.04                        ATOM 3266 CA VAL A 431 0 -0.956 25.713 37.966 1.00 22.61                      ATOM 3267 C VAL A 431 0 -1.337 26.028 39.409 1.00 23.06                       ATOM 3268 O VAL A 431 0 -0.476 26.392 40.218 1.00 22.42                       ATOM 3269 CB VAL A 431 0 -1.245 24.193 37.768 1.00 23.03                      ATOM 3270 CG1 VAL A 431 0 -0.795 23.672 36.416 1.00 22.74                     ATOM 3271 CG2 VAL A 431 0 -0.574 23.315 38.820 1.00 22.77                     ATOM 3272 N THR A 432 0 -2.615 25.835 39.704 1.00 23.88                       ATOM 3273 CA THR A 432 0 -3.168 26.067 41.041 1.00 24.18                      ATOM 3274 C THR A 432 0 -2.324 25.401 42.092 1.00 23.94                       ATOM 3275 O THR A 432 0 -1.915 24.249 41.909 1.00 24.69                       ATOM 3276 CB THR A 432 0 -4.625 25.565 41.069 1.00 25.75                      ATOM 3277 OG1 THR A 432 0 -5.336 26.344 40.087 1.00 25.87                     ATOM 3278 CG2 THR A 432 0 -5.319 25.800 42.398 1.00 26.65                     ATOM 3279 N GLY A 433 0 -1.924 26.136 43.124 1.00 24.45                       ATOM 3280 CA GLY A 433 0 -1.035 25.589 44.159 1.00 22.27                      ATOM 3281 C GLY A 433 0 0.394 26.120 43.983 1.00 23.26                        ATOM 3282 O GLY A 433 0 1.103 26.212 45.000 1.00 23.30                        ATOM 3283 N ASP A 434 0 0.833 26.481 42.776 1.00 21.12                        ATOM 3284 CA ASP A 434 0 2.192 26.986 42.586 1.00 20.62                       ATOM 3285 C ASP A 434 0 2.360 28.408 43.126 1.00 22.36                        ATOM 3286 O ASP A 434 0 1.425 29.225 43.076 1.00 21.24                        ATOM 3287 CB ASP A 434 0 2.548 27.024 41.087 1.00 18.78                       ATOM 3288 CG ASP A 434 0 2.827 25.616 40.597 1.00 19.71                       ATOM 3289 OD1 ASP A 434 0 3.304 24.828 41.409 1.00 20.43                      ATOM 3290 OD2 ASP A 434 0 2.596 25.242 39.432 1.00 21.58                      ATOM 3291 N GLU A 435 0 3.585 28.721 43.562 1.00 22.08                        ATOM 3292 CA GLU A 435 0 3.853 30.077 44.068 1.00 23.24                       ATOM 3293 C GLU A 435 0 5.244 30.512 43.612 1.00 20.24                        ATOM 3294 O GLU A 435 0 6.201 30.611 44.372 1.00 19.50                        ATOM 3295 CB GLU A 435 0 3.659 30.068 45.572 1.00 25.56                       ATOM 3296 CG GLU A 435 0 3.739 31.409 46.258 1.00 30.52                       ATOM 3297 CD GLU A 435 0 3.107 31.350 47.657 1.00 35.00                       ATOM 3298 OE1 GLU A 435 0 2.093 30.603 47.760 1.00 35.71                      ATOM 3299 OE2 GLU A 435 0 3.658 32.020 48.579 1.00 35.91                      ATOM 3300 N VAL A 436 0 5.344 30.690 42.297 1.00 17.80                        ATOM 3301 CA VAL A 436 0 6.564 31.083 41.640 1.00 15.30                       ATOM 3302 C VAL A 436 0 7.049 32.416 42.221 1.00 17.15                        ATOM 3303 O VAL A 436 0 6.326 33.402 42.275 1.00 17.48                        ATOM 3304 CB VAL A 436 0 6.360 31.219 40.129 1.00 14.63                       ATOM 3305 CG1 VAL A 436 0 7.463 32.009 39.454 1.00 10.79                      ATOM 3306 CG2 VAL A 436 0 6.238 29.806 39.536 1.00 14.13                      ATOM 3307 N THR A 437 0 8.290 32.391 42.691 1.00 16.51                        ATOM 3308 CA THR A 437 0 8.940 33.505 43.364 1.00 16.19                       ATOM 3309 C THR A 437 0 10.254 33.817 42.668 1.00 15.24                       ATOM 3310 O THR A 437 0 11.100 32.940 42.419 1.00 15.47                       ATOM 3311 CB THR A 437 0 9.190 33.067 44.827 1.00 14.95                       ATOM 3312 OG1 THR A 437 0 7.969 32.499 45.308 1.00 13.50                      ATOM 3313 CG2 THR A 437 0 9.599 34.232 45.697 1.00 13.41                      ATOM 3314 N ILE A 438 0 10.413 35.059 42.251 1.00 13.38                       ATOM 3315 CA ILE A 438 0 11.597 35.471 41.510 1.00 15.78                      ATOM 3316 C ILE A 438 0 12.292 36.590 42.264 1.00 15.86                       ATOM 3317 O ILE A 438 0 11.617 37.270 43.048 1.00 17.32                       ATOM 3318 CB ILE A 438 0 11.249 35.848 40.053 1.00 15.40                      ATOM 3319 CG1 ILE A 438 0 10.340 37.055 39.985 1.00 15.85                     ATOM 3320 CG2 ILE A 438 0 10.602 34.653 39.346 1.00 17.11                     ATOM 3321 CD1 ILE A 438 0 9.971 37.607 38.632 1.00 17.49                      ATOM 3322 N ARG A 439 0 13.599 36.789 42.055 1.00 16.02                       ATOM 3323 CA ARG A 439 0 14.315 37.896 42.671 1.00 13.90                      ATOM 3324 C ARG A 439 0 15.181 38.645 41.676 1.00 13.52                       ATOM 3325 O ARG A 439 0 15.748 38.056 40.762 1.00 14.74                       ATOM 3326 CB ARG A 439 0 15.193 37.501 43.850 1.00 15.15                      ATOM 3327 CG ARG A 439 0 14.457 37.235 45.147 1.00 14.83                      ATOM 3328 CD ARG A 439 0 15.367 37.337 46.355 1.00 14.08                      ATOM 3329 NE ARG A 439 0 14.613 37.000 47.566 1.00 17.06                      ATOM 3330 CZ ARG A 439 0 15.192 36.922 48.767 1.00 18.01                      ATOM 3331 NH1 ARG A 439 0 16.487 37.176 48.908 1.00 17.76                     ATOM 3332 NH2 ARG A 439 0 14.459 36.604 49.818 1.00 18.55                     ATOM 3333 N PHE A 440 0 15.314 39.957 41.853 1.00 14.44                       ATOM 3334 CA PHE A 440 0 16.204 40.737 40.993 1.00 15.97                      ATOM 3335 C PHE A 440 0 16.645 41.986 41.761 1.00 15.86                       ATOM 3336 O PHE A 440 0 16.113 42.313 42.801 1.00 15.79                       ATOM 3337 CB PHE A 440 0 15.638 41.081 39.620 1.00 15.17                      ATOM 3338 CG PHE A 440 0 14.416 41.948 39.647 1.00 16.95                      ATOM 3339 CD1 PHE A 440 0 14.525 43.333 39.528 1.00 17.23                     ATOM 3340 CD2 PHE A 440 0 13.158 41.377 39.798 1.00 16.35                     ATOM 3341 CE1 PHE A 440 0 13.397 44.152 39.566 1.00 17.07                     ATOM 3342 CE2 PHE A 440 0 12.026 42.180 39.841 1.00 17.12                     ATOM 3343 CZ PHE A 440 0 12.144 43.575 39.719 1.00 18.30                      ATOM 3344 N VAL A 441 0 17.676 42.648 41.268 1.00 16.10                       ATOM 3345 CA VAL A 441 0 18.172 43.874 41.879 1.00 16.29                      ATOM 3346 C VAL A 441 0 17.776 45.035 40.972 1.00 14.00                       ATOM 3347 O VAL A 441 0 17.866 44.924 39.736 1.00 12.72                       ATOM 3348 CB VAL A 441 0 19.675 43.769 42.144 1.00 18.13                      ATOM 3349 CG1 VAL A 441 0 20.195 45.040 42.794 1.00 18.53                     ATOM 3350 CG2 VAL A 441 0 19.969 42.583 43.065 1.00 18.55                     ATOM 3351 N THR A 442 0 17.328 46.125 41.579 1.00 11.73                       ATOM 3352 CA THR A 442 0 16.905 47.291 40.800 1.00 13.02                      ATOM 3353 C THR A 442 0 18.055 48.208 40.432 1.00 14.83                       ATOM 3354 O THR A 442 0 18.218 49.323 40.947 1.00 15.17                       ATOM 3355 CB THR A 442 0 15.840 48.127 41.558 1.00 14.62                      ATOM 3356 OG1 THR A 442 0 16.314 48.463 42.864 1.00 14.34                     ATOM 3357 CG2 THR A 442 0 14.552 47.299 41.727 1.00 13.82                     ATOM 3358 N ASP A 443 0 18.818 47.764 39.437 1.00 15.48                       ATOM 3359 CA ASP A 443 0 20.004 48.449 38.964 1.00 16.57                      ATOM 3360 C ASP A 443 0 19.807 49.010 37.569 1.00 15.38                       ATOM 3361 O ASP A 443 0 20.788 49.208 36.858 1.00 15.57                       ATOM 3362 CB ASP A 443 0 21.133 47.391 38.962 1.00 19.75                      ATOM 3363 CG ASP A 443 0 20.877 46.264 37.990 1.00 22.78                      ATOM 3364 OD1 ASP A 443 0 21.711 45.353 37.789 1.00 25.70                     ATOM 3365 OD2 ASP A 443 0 19.836 46.161 37.313 1.00 23.88                     ATOM 3366 N ASN A 444 0 18.593 49.278 37.144 1.00 13.71                       ATOM 3367 CA ASN A 444 0 18.388 49.721 35.752 1.00 15.87                      ATOM 3368 C ASN A 444 0 17.245 50.728 35.702 1.00 17.00                       ATOM 3369 O ASN A 444 0 16.052 50.419 35.614 1.00 16.83                       ATOM 3370 CB ASN A 444 0 18.198 48.453 34.930 1.00 15.78                      ATOM 3371 CG ASN A 444 0 18.225 48.675 33.442 1.00 18.49                      ATOM 3372 OD1 ASN A 444 0 18.505 49.809 33.047 1.00 19.42                     ATOM 3373 ND2 ASN A 444 0 17.925 47.689 32.588 1.00 15.91                     ATOM 3374 N PRO A 445 0 17.598 52.003 35.890 1.00 17.59                       ATOM 3375 CA PRO A 445 0 16.683 53.137 35.938 1.00 16.56                      ATOM 3376 C PRO A 445 0 15.788 53.217 34.721 1.00 16.99                       ATOM 3377 O PRO A 445 0 16.293 53.246 33.594 1.00 17.02                       ATOM 3378 CB PRO A 445 0 17.552 54.418 35.951 1.00 18.28                      ATOM 3379 CG PRO A 445 0 18.870 53.871 36.474 1.00 18.09                      ATOM 3380 CD PRO A 445 0 19.002 52.409 36.084 1.00 16.05                      ATOM 3381 N GLY A 446 0 14.462 53.194 34.918 1.00 17.16                       ATOM 3382 CA GLY A 446 0 13.560 53.281 33.743 1.00 15.84                      ATOM 3383 C GLY A 446 0 12.297 52.453 33.984 1.00 14.24                       ATOM 3384 O GLY A 446 0 12.192 51.797 35.005 1.00 12.22                       ATOM 3385 N PRO A 447 0 11.285 52.697 33.181 1.00 15.53                       ATOM 3386 CA PRO A 447 0 9.999 52.048 33.195 1.00 15.24                       ATOM 3387 C PRO A 447 0 10.101 50.737 32.401 1.00 13.82                       ATOM 3388 O PRO A 447 0 10.514 50.733 31.240 1.00 13.85                       ATOM 3389 CB PRO A 447 0 9.013 52.976 32.473 1.00 16.21                       ATOM 3390 CG PRO A 447 0 9.933 53.729 31.554 1.00 16.19                       ATOM 3391 CD PRO A 447 0 11.347 53.707 32.096 1.00 17.15                      ATOM 3392 N TRP A 448 0 9.787 49.623 33.021 1.00 11.83                        ATOM 3393 CA TRP A 448 0 9.898 48.317 32.371 1.00 14.30                       ATOM 3394 C TRP A 448 0 8.610 47.493 32.427 1.00 13.12                        ATOM 3395 O TRP A 448 0 8.013 47.355 33.502 1.00 11.63                        ATOM 3396 CB TRP A 448 0 10.985 47.483 33.095 1.00 13.17                      ATOM 3397 CG TRP A 448 0 12.321 48.160 33.124 1.00 14.54                      ATOM 3398 CD1 TRP A 448 0 12.897 48.728 34.239 1.00 14.19                     ATOM 3399 CD2 TRP A 448 0 13.211 48.382 32.029 1.00 14.38                     ATOM 3400 NE1 TRP A 448 0 14.083 49.290 33.873 1.00 15.02                     ATOM 3401 CE2 TRP A 448 0 14.308 49.095 32.527 1.00 14.41                     ATOM 3402 CE3 TRP A 448 0 13.193 48.053 30.672 1.00 15.39                     ATOM 3403 CZ2 TRP A 448 0 15.388 49.467 31.729 1.00 14.57                     ATOM 3404 CZ3 TRP A 448 0 14.250 48.446 29.867 1.00 14.92                     ATOM 3405 CH2 TRP A 448 0 15.355 49.135 30.399 1.00 14.93                     ATOM 3406 N PHE A 449 0 8.231 46.884 31.315 1.00 14.03                        ATOM 3407 CA PHE A 449 0 7.023 46.039 31.297 1.00 13.60                       ATOM 3408 C PHE A 449 0 7.231 44.712 32.016 1.00 15.32                        ATOM 3409 O PHE A 449 0 8.312 44.093 31.993 1.00 13.66                        ATOM 3410 CB PHE A 449 0 6.627 45.773 29.845 1.00 16.19                       ATOM 3411 CG PHE A 449 0 5.221 46.033 29.380 1.00 18.26                       ATOM 3412 CD1 PHE A 449 0 4.165 46.288 30.226 1.00 17.95                      ATOM 3413 CD2 PHE A 449 0 4.962 46.027 28.011 1.00 20.73                      ATOM 3414 CE1 PHE A 449 0 2.899 46.565 29.745 1.00 18.55                      ATOM 3415 CE2 PHE A 449 0 3.701 46.293 27.503 1.00 20.13                      ATOM 3416 CZ PHE A 449 0 2.664 46.543 28.387 1.00 18.59                       ATOM 3417 N PHE A 450 0 6.195 44.245 32.715 1.00 12.79                        ATOM 3418 CA PHE A 450 0 6.119 42.963 33.359 1.00 14.38                       ATOM 3419 C PHE A 450 0 4.775 42.323 32.952 1.00 15.45                        ATOM 3420 O PHE A 450 0 3.743 42.812 33.423 1.00 15.30                        ATOM 3421 CB PHE A 450 0 6.186 43.041 34.879 1.00 15.06                       ATOM 3422 CG PHE A 450 0 6.210 41.693 35.555 1.00 15.95                       ATOM 3423 CD1 PHE A 450 0 7.157 40.734 35.204 1.00 16.36                      ATOM 3424 CD2 PHE A 450 0 5.325 41.398 36.570 1.00 15.45                      ATOM 3425 CE1 PHE A 450 0 7.222 39.518 35.855 1.00 13.87                      ATOM 3426 CE2 PHE A 450 0 5.386 40.187 37.224 1.00 16.10                      ATOM 3427 CZ PHE A 450 0 6.317 39.236 36.854 1.00 15.90                       ATOM 3428 N HIS A 451 0 4.737 41.301 32.122 1.00 15.54                        ATOM 3429 CA HIS A 451 0 3.443 40.841 31.610 1.00 16.24                       ATOM 3430 C HIS A 451 0 3.461 39.426 31.073 1.00 16.95                        ATOM 3431 O HIS A 451 0 4.526 38.860 30.812 1.00 17.42                        ATOM 3432 CB HIS A 451 0 2.996 41.743 30.435 1.00 14.01                       ATOM 3433 CG HIS A 451 0 3.921 41.696 29.281 1.00 16.98                       ATOM 3434 ND1 HIS A 451 0 3.791 40.844 28.201 1.00 18.14                      ATOM 3435 CD2 HIS A 451 0 5.058 42.435 29.046 1.00 17.88                      ATOM 3436 CE1 HIS A 451 0 4.759 41.060 27.337 1.00 17.83                      ATOM 3437 NE2 HIS A 451 0 5.554 42.011 27.842 1.00 18.98                      ATOM 3438 N CYS A 452 0 2.261 38.863 30.951 1.00 16.78                        ATOM 3439 CA CYS A 452 0 2.167 37.537 30.388 1.00 16.34                       ATOM 3440 C CYS A 452 0 2.604 37.623 28.924 1.00 14.77                        ATOM 3441 O CYS A 452 0 2.167 38.514 28.188 1.00 13.61                        ATOM 3442 CB CYS A 452 0 0.727 36.983 30.451 1.00 18.22                       ATOM 3443 SG CYS A 452 0 0.701 35.325 29.692 1.00 19.80                       ATOM 3444 N HIS A 453 0 3.388 36.640 28.474 1.00 13.29                        ATOM 3445 CA HIS A 453 0 3.867 36.716 27.100 1.00 13.19                       ATOM 3446 C HIS A 453 0 2.983 35.987 26.099 1.00 13.47                        ATOM 3447 O HIS A 453 0 3.296 35.974 24.906 1.00 11.93                        ATOM 3448 CB HIS A 453 0 5.314 36.251 27.033 1.00 13.98                       ATOM 3449 CG HIS A 453 0 6.124 36.860 25.945 1.00 11.89                       ATOM 3450 ND1 HIS A 453 0 5.835 36.763 24.612 1.00 10.68                      ATOM 3451 CD2 HIS A 453 0 7.270 37.594 26.072 1.00 12.71                      ATOM 3452 CE1 HIS A 453 0 6.776 37.418 23.923 1.00 12.37                      ATOM 3453 NE2 HIS A 453 0 7.663 37.930 24.793 1.00 13.20                      ATOM 3454 N ILE A 454 0 1.860 35.429 26.549 1.00 15.35                        ATOM 3455 CA ILE A 454 0 0.849 34.937 25.600 1.00 15.85                       ATOM 3456 C ILE A 454 0 0.214 36.238 25.089 1.00 18.65                        ATOM 3457 O ILE A 454 0 -0.452 36.997 25.824 1.00 17.92                       ATOM 3458 CB ILE A 454 0 -0.156 34.001 26.280 1.00 16.46                      ATOM 3459 CG1 ILE A 454 0 0.456 32.598 26.512 1.00 15.26                      ATOM 3460 CG2 ILE A 454 0 -1.402 33.898 25.419 1.00 14.21                     ATOM 3461 CD1 ILE A 454 0 -0.249 31.804 27.592 1.00 16.26                     ATOM 3462 N GLU A 455 0 0.448 36.607 23.832 1.00 21.02                        ATOM 3463 CA GLU A 455 0 -0.024 37.856 23.289 1.00 23.78                      ATOM 3464 C GLU A 455 0 -1.526 38.042 23.422 1.00 24.40                       ATOM 3465 O GLU A 455 0 -1.953 39.161 23.700 1.00 24.30                       ATOM 3466 CB GLU A 455 0 0.399 38.090 21.830 1.00 27.20                       ATOM 3467 CG GLU A 455 0 0.602 39.599 21.595 1.00 33.86                       ATOM 3468 CD GLU A 455 0 1.783 40.205 22.309 1.00 37.49                       ATOM 3469 OE1 GLU A 455 0 2.311 39.657 23.320 1.00 41.51                      ATOM 3470 OE2 GLU A 455 0 2.303 41.284 21.907 1.00 41.22                      ATOM 3471 N PHE A 456 0 -2.347 37.005 23.334 1.00 23.97                       ATOM 3472 CA PHE A 456 0 -3.775 37.163 23.516 1.00 24.68                      ATOM 3473 C PHE A 456 0 -4.084 37.533 24.959 1.00 25.11                       ATOM 3474 O PHE A 456 0 -5.181 38.092 25.170 1.00 27.37                       ATOM 3475 CB PHE A 456 0 -4.552 35.919 23.023 1.00 24.76                      ATOM 3476 CG PHE A 456 0 -4.098 35.614 21.606 1.00 24.98                      ATOM 3477 CD1 PHE A 456 0 -4.392 36.500 20.590 1.00 24.98                     ATOM 3478 CD2 PHE A 456 0 -3.331 34.506 21.320 1.00 24.42                     ATOM 3479 CE1 PHE A 456 0 -3.988 36.292 19.291 1.00 25.44                     ATOM 3480 CE2 PHE A 456 0 -2.913 34.293 20.015 1.00 26.40                     ATOM 3481 CZ PHE A 456 0 -3.226 35.171 18.997 1.00 25.10                      ATOM 3482 N HIS A 457 0 -3.205 37.294 25.922 1.00 22.35                       ATOM 3483 CA HIS A 457 0 -3.508 37.682 27.291 1.00 22.55                      ATOM 3484 C HIS A 457 0 -3.053 39.121 27.561 1.00 23.81                       ATOM 3485 O HIS A 457 0 -3.756 39.832 28.262 1.00 21.33                       ATOM 3486 CB HIS A 457 0 -2.912 36.766 28.336 1.00 20.96                      ATOM 3487 CG HIS A 457 0 -3.345 35.346 28.201 1.00 22.51                      ATOM 3488 ND1 HIS A 457 0 -2.745 34.329 28.905 1.00 21.40                     ATOM 3489 CD2 HIS A 457 0 -4.291 34.771 27.404 1.00 22.50                     ATOM 3490 CE1 HIS A 457 0 -3.320 33.184 28.575 1.00 22.51                     ATOM 3491 NE2 HIS A 457 0 -4.237 33.428 27.666 1.00 23.19                     ATOM 3492 N LEU A 458 0 -1.876 39.481 27.028 1.00 23.74                       ATOM 3493 CA LEU A 458 0 -1.357 40.817 27.125 1.00 24.76                      ATOM 3494 C LEU A 458 0 -2.411 41.828 26.616 1.00 26.52                       ATOM 3495 O LEU A 458 0 -2.757 42.751 27.351 1.00 25.18                       ATOM 3496 CB LEU A 458 0 -0.108 40.986 26.252 1.00 23.81                      ATOM 3497 CG LEU A 458 0 0.898 42.062 26.624 1.00 24.09                       ATOM 3498 CD1 LEU A 458 0 1.619 42.606 25.390 1.00 24.28                      ATOM 3499 CD2 LEU A 458 0 0.351 43.195 27.462 1.00 23.72                      ATOM 3500 N MET A 459 0 -2.896 41.611 25.388 1.00 28.19                       ATOM 3501 CA MET A 459 0 -3.914 42.458 24.785 1.00 31.98                      ATOM 3502 C MET A 459 0 -5.207 42.436 25.603 1.00 29.95                       ATOM 3503 O MET A 459 0 -5.886 43.439 25.520 1.00 29.10                       ATOM 3504 CB MET A 459 0 -4.148 42.226 23.284 1.00 35.99                      ATOM 3505 CG MET A 459 0 -5.056 41.103 22.852 1.00 42.66                      ATOM 3506 SD MET A 459 0 -5.296 40.817 21.069 1.00 49.28                      ATOM 3507 CE MET A 459 0 -6.238 39.291 21.119 1.00 47.39                      ATOM 3508 N ASN A 460 0 -5.523 41.486 26.464 1.00 29.07                       ATOM 3509 CA ASN A 460 0 -6.706 41.539 27.296 1.00 29.41                      ATOM 3510 C ASN A 460 0 -6.407 41.908 28.746 1.00 28.46                       ATOM 3511 O ASN A 460 0 -7.183 41.577 29.645 1.00 26.89                       ATOM 3512 CB ASN A 460 0 -7.537 40.253 27.210 1.00 31.34                      ATOM 3513 CG ASN A 460 0 -8.325 40.243 25.900 1.00 33.82                      ATOM 3514 OD1 ASN A 460 0 -7.909 39.609 24.926 1.00 34.29                     ATOM 3515 ND2 ASN A 460 0 -9.437 40.971 25.861 1.00 34.55                     ATOM 3516 N GLY A 461 0 -5.320 42.655 28.981 1.00 26.30                       ATOM 3517 CA GLY A 461 0 -5.020 43.198 30.268 1.00 24.99                      ATOM 3518 C GLY A 461 0 -4.043 42.601 31.235 1.00 24.75                       ATOM 3519 0 GLY A 461 0 -3.879 43.228 32.304 1.00 22.69                       ATOM 3520 N LEU A 462 0 -3.375 41.478 30.914 1.00 22.85                       ATOM 3521 CA LEU A 462 0 -2.478 40.872 31.913 1.00 22.10                      ATOM 3522 C LEU A 462 0 -1.071 41.485 31.890 1.00 21.56                       ATOM 3523 O LEU A 462 0 -0.116 40.876 31.415 1.00 20.28                       ATOM 3524 CB LEU A 462 0 -2.477 39.376 31.669 1.00 20.03                      ATOM 3525 CG LEU A 462 0 -2.010 38.393 32.720 1.00 20.40                      ATOM 3526 CD1 LEU A 462 0 -2.603 38.608 34.093 1.00 20.35                     ATOM 3527 CD2 LEU A 462 0 -2.385 36.983 32.229 1.00 21.01                     ATOM 3528 N ALA A 463 0 -0.908 42.695 32.408 1.00 20.00                       ATOM 3529 CA ALA A 463 0 0.350 43.432 32.381 1.00 20.74                       ATOM 3530 C ALA A 463 0 0.398 44.511 33.481 1.00 21.85                        ATOM 3531 O ALA A 463 0 -0.667 44.965 33.934 1.00 22.85                       ATOM 3532 CB ALA A 463 0 0.559 44.179 31.060 1.00 15.13                       ATOM 3533 N ILE A 464 0 1.605 44.810 33.950 1.00 19.91                        ATOM 3534 CA ILE A 464 0 1.852 45.905 34.850 1.00 19.81                       ATOM 3535 C ILE A 464 0 3.180 46.579 34.434 1.00 19.41                        ATOM 3536 O ILE A 464 0 3.938 46.003 33.660 1.00 18.24                        ATOM 3537 CB ILE A 464 0 1.910 45.678 36.347 1.00 19.13                       ATOM 3538 CG1 ILE A 464 0 2.867 44.546 36.697 1.00 19.39                      ATOM 3539 CG2 ILE A 464 0 0.520 45.455 36.924 1.00 18.48                      ATOM 3540 CD1 ILE A 464 0 3.205 44.549 38.179 1.00 21.00                      ATOM 3541 N VAL A 465 0 3.380 47.791 34.924 1.00 18.95                        ATOM 3542 CA VAL A 465 0 4.579 48.570 34.637 1.00 18.36                       ATOM 3543 C VAL A 465 0 5.327 48.928 35.931 1.00 18.07                        ATOM 3544 O VAL A 465 0 4.787 49.424 36.931 1.00 15.19                        ATOM 3545 CB VAL A 465 0 4.329 49.913 33.918 1.00 19.73                       ATOM 3546 CG1 VAL A 465 0 5.659 50.605 33.602 1.00 18.34                      ATOM 3547 CG2 VAL A 465 0 3.522 49.766 32.629 1.00 18.74                      ATOM 3548 N PHE A 466 0 6.649 48.655 35.879 1.00 17.55                        ATOM 3549 CA PHE A 466 0 7.499 49.051 37.013 1.00 14.72                       ATOM 3550 C PHE A 466 0 8.251 50.344 36.653 1.00 12.68                        ATOM 3551 O PHE A 466 0 9.007 50.420 35.679 1.00 12.23                        ATOM 3552 CB PHE A 466 0 8.484 47.978 37.381 1.00 15.19                       ATOM 3553 CG PHE A 466 0 7.962 46.770 38.080 1.00 15.90                       ATOM 3554 CD1 PHE A 466 0 7.328 46.856 39.299 1.00 16.23                      ATOM 3555 CD2 PHE A 466 0 8.153 45.533 37.492 1.00 16.23                      ATOM 3556 CE1 PHE A 466 0 6.861 45.720 39.936 1.00 15.97                      ATOM 3557 CE2 PHE A 466 0 7.665 44.389 38.133 1.00 18.27                      ATOM 3558 CZ PHE A 466 0 7.018 44.480 39.352 1.00 16.74                       ATOM 3559 N ALA A 467 0 8.045 51.361 37.443 1.00 10.60                        ATOM 3560 CA ALA A 467 0 8.788 52.648 37.194 1.00 12.27                       ATOM 3561 C ALA A 467 0 10.007 52.526 38.111 1.00 12.02                       ATOM 3562 O ALA A 467 0 9.905 52.728 39.325 1.00 12.43                        ATOM 3563 CB ALA A 467 0 7.845 53.790 37.501 1.00 10.50                       ATOM 3564 N GLU A 468 0 11.126 51.989 37.625 1.00 12.62                       ATOM 3565 CA GLU A 468 0 12.263 51.683 38.515 1.00 14.63                      ATOM 3566 C GLU A 468 0 13.195 52.883 38.685 1.00 13.91                       ATOM 3567 O GLU A 468 0 13.631 53.369 37.651 1.00 13.05                       ATOM 3568 CB GLU A 468 0 13.049 50.546 37.843 1.00 14.51                      ATOM 3569 CG GLU A 468 0 14.256 50.035 38.629 1.00 16.84                      ATOM 3570 CD GLU A 468 0 14.805 48.779 37.975 1.00 17.96                      ATOM 3571 OE1 GLU A 468 0 15.985 48.479 38.124 1.00 16.98                     ATOM 3572 OE2 GLU A 468 0 14.086 48.043 37.260 1.00 18.42                     ATOM 3573 N ASP A 469 0 13.546 53.286 39.886 1.00 15.17                       ATOM 3574 CA ASP A 469 0 14.491 54.371 40.116 1.00 16.85                      ATOM 3575 C ASP A 469 0 14.134 55.630 39.333 1.00 16.33                       ATOM 3576 O ASP A 469 0 14.851 56.046 38.437 1.00 16.59                       ATOM 3577 CB ASP A 469 0 15.899 53.920 39.748 1.00 19.86                      ATOM 3578 CG ASP A 469 0 17.040 54.766 40.289 1.00 21.40                      ATOM 3579 OD1 ASP A 469 0 16.811 55.793 40.943 1.00 22.21                     ATOM 3580 OD2 ASP A 469 0 18.216 54.403 40.069 1.00 22.21                     ATOM 3581 N MET A 470 0 13.007 56.246 39.635 1.00 16.12                       ATOM 3582 CA MET A 470 0 12.522 57.373 38.853 1.00 18.77                      ATOM 3583 C MET A 470 0 13.451 58.576 38.950 1.00 16.31                       ATOM 3584 O MET A 470 0 13.591 59.208 37.925 1.00 13.55                       ATOM 3585 CB MET A 470 0 11.116 57.847 39.302 1.00 20.06                      ATOM 3586 CG MET A 470 0 10.041 56.941 38.684 1.00 23.99                      ATOM 3587 SD MET A 470 0 8.375 57.337 39.283 1.00 26.08                       ATOM 3588 CE MET A 470 0 8.030 58.581 38.020 1.00 24.40                       ATOM 3589 N ALA A 471 0 14.046 58.793 40.117 1.00 14.69                       ATOM 3590 CA ALA A 471 0 14.953 59.906 40.287 1.00 16.97                      ATOM 3591 C ALA A 471 0 16.141 59.864 39.335 1.00 18.79                       ATOM 3592 O ALA A 471 0 16.602 60.956 38.945 1.00 21.08                       ATOM 3593 CB ALA A 471 0 15.471 59.927 41.728 1.00 17.62                      ATOM 3594 N ASN A 472 0 16.623 58.695 38.912 1.00 17.28                       ATOM 3595 CA ASN A 472 0 17.788 58.675 38.015 1.00 16.56                      ATOM 3596 C ASN A 472 0 17.457 58.355 36.572 1.00 16.99                       ATOM 3597 O ASN A 472 0 18.407 58.143 35.795 1.00 18.74                       ATOM 3598 CB ASN A 472 0 18.811 57.645 38.548 1.00 14.60                      ATOM 3599 CG ASN A 472 0 19.417 58.132 39.887 1.00 14.00                      ATOM 3600 OD1 ASN A 472 0 18.895 57.830 40.967 1.00 12.71                     ATOM 3601 ND2 ASN A 472 0 20.468 58.916 39.775 1.00 10.80                     ATOM 3602 N THR A 473 0 16.174 58.284 36.239 1.00 14.26                       ATOM 3603 CA THR A 473 0 15.789 57.885 34.882 1.00 15.82                      ATOM 3604 C THR A 473 0 16.150 58.891 33.812 1.00 16.81                       ATOM 3605 O THR A 473 0 16.599 58.455 32.746 1.00 15.89                       ATOM 3606 CB THR A 473 0 14.267 57.576 34.826 1.00 16.10                      ATOM 3607 OG1 THR A 473 0 14.001 56.416 35.609 1.00 15.41                     ATOM 3608 CG2 THR A 473 0 13.750 57.337 33.427 1.00 15.24                     ATOM 3609 N VAL A 474 0 16.000 60.195 34.081 1.00 18.57                       ATOM 3610 CA VAL A 474 0 16.355 61.192 33.050 1.00 21.06                      ATOM 3611 C VAL A 474 0 17.859 61.209 32.817 1.00 19.12                       ATOM 3612 O VAL A 474 0 18.339 61.234 31.688 1.00 19.95                       ATOM 3613 CB VAL A 474 0 15.860 62.616 33.424 1.00 22.91                      ATOM 3614 CG1 VAL A 474 0 16.467 63.702 32.538 1.00 23.06                     ATOM 3615 CG2 VAL A 474 0 14.346 62.721 33.334 1.00 23.04                     ATOM 3616 N ASP A 475 0 18.647 61.175 33.886 1.00 19.20                       ATOM 3617 CA ASP A 475 0 20.109 61.168 33.741 1.00 18.98                      ATOM 3618 C ASP A 475 0 20.578 59.899 33.047 1.00 17.52                       ATOM 3619 O ASP A 475 0 21.386 60.028 32.130 1.00 18.31                       ATOM 3620 CB ASP A 475 0 20.780 61.273 35.119 1.00 20.27                      ATOM 3621 CG ASP A 475 0 22.283 61.075 35.107 1.00 20.18                      ATOM 3622 OD1 ASP A 475 0 22.950 61.889 34.431 1.00 21.73                     ATOM 3623 OD2 ASP A 475 0 22.798 60.139 35.750 1.00 18.03                     ATOM 3624 N ALA A 476 0 20.062 58.725 33.392 1.00 18.26                       ATOM 3625 CA ALA A 476 0 20.539 57.486 32.793 1.00 18.93                      ATOM 3626 C ALA A 476 0 20.165 57.269 31.343 1.00 20.62                       ATOM 3627 O ALA A 476 0 20.845 56.502 30.661 1.00 22.64                       ATOM 3628 CB ALA A 476 0 19.966 56.298 33.551 1.00 18.48                      ATOM 3629 N ASN A 477 0 19.047 57.787 30.858 1.00 22.66                       ATOM 3630 CA ASN A 477 0 18.605 57.512 29.491 1.00 25.22                      ATOM 3631 C ASN A 477 0 18.578 58.782 28.683 1.00 28.55                       ATOM 3632 O ASN A 477 0 17.969 59.755 29.143 1.00 30.20                       ATOM 3633 CB ASN A 477 0 17.172 56.948 29.560 1.00 24.22                      ATOM 3634 CG ASN A 477 0 17.114 55.666 30.380 1.00 23.73                      ATOM 3635 OD1 ASN A 477 0 16.747 55.672 31.570 1.00 21.33                     ATOM 3636 ND2 ASN A 477 0 17.512 54.575 29.736 1.00 20.87                     ATOM 3637 N ASN A 478 0 19.208 58.878 27.514 1.00 31.69                       ATOM 3638 CA ASN A 478 0 19.036 60.131 26.776 1.00 33.61                      ATOM 3639 C ASN A 478 0 18.758 59.770 25.331 1.00 32.22                       ATOM 3640 O ASN A 478 0 19.602 59.478 24.508 1.00 32.16                       ATOM 3641 CB ASN A 478 0 20.086 61.194 27.017 1.00 38.57                      ATOM 3642 CG ASN A 478 0 21.426 60.602 27.370 1.00 40.94                      ATOM 3643 OD1 ASN A 478 0 21.928 59.903 26.484 1.00 44.60                     ATOM 3644 ND2 ASN A 478 0 21.866 60.861 28.578 1.00 41.32                     ATOM 3645 N PRO A 479 0 17.461 59.733 25.075 1.00 32.37                       ATOM 3646 CA PRO A 479 0 16.890 59.381 23.790 1.00 31.84                      ATOM 3647 C PRO A 479 0 17.268 60.448 22.776 1.00 32.35                       ATOM 3648 O PRO A 479 0 17.422 61.609 23.136 1.00 32.66                       ATOM 3649 CB PRO A 479 0 15.364 59.385 23.931 1.00 31.68                      ATOM 3650 CG PRO A 479 0 15.126 59.724 25.373 1.00 31.69                      ATOM 3651 CD PRO A 479 0 16.416 60.071 26.064 1.00 32.23                      ATOM 3652 N PRO A 480 0 17.399 60.036 21.537 1.00 31.62                       ATOM 3653 CA PRO A 480 0 17.670 60.939 20.422 1.00 30.72                      ATOM 3654 C PRO A 480 0 16.452 61.827 20.225 1.00 30.37                       ATOM 3655 O PRO A 480 0 15.362 61.525 20.733 1.00 29.47                       ATOM 3656 CB PRO A 480 0 17.935 60.035 19.203 1.00 29.87                      ATOM 3657 CG PRO A 480 0 17.111 58.811 19.590 1.00 30.44                      ATOM 3658 CD PRO A 480 0 17.161 58.657 21.093 1.00 30.35                      ATOM 3659 N VAL A 481 0 16.559 62.906 19.458 1.00 31.72                       ATOM 3660 CA VAL A 481 0 15.398 63.788 19.268 1.00 30.68                      ATOM 3661 C VAL A 481 0 14.335 63.090 18.446 1.00 29.51                       ATOM 3662 O VAL A 481 0 13.134 63.284 18.648 1.00 27.97                       ATOM 3663 CB VAL A 481 0 15.818 65.132 18.648 1.00 33.04                      ATOM 3664 CG1 VAL A 481 0 16.126 65.010 17.161 1.00 31.91                     ATOM 3665 CG2 VAL A 481 0 14.717 66.171 18.907 1.00 33.32                     ATOM 3666 N GLU A 482 0 14.746 62.167 17.562 1.00 28.90                       ATOM 3667 CA GLU A 482 0 13.755 61.402 16.803 1.00 29.62                      ATOM 3668 C GLU A 482 0 12.839 60.565 17.691 1.00 28.33                       ATOM 3669 O GLU A 482 0 11.704 60.287 17.280 1.00 28.36                       ATOM 3670 CB GLU A 482 0 14.449 60.498 15.788 1.00 30.63                      ATOM 3671 CG GLU A 482 0 15.143 61.256 14.666 1.00 32.78                      ATOM 3672 CD GLU A 482 0 16.522 61.784 14.990 1.00 34.96                      ATOM 3673 OE1 GLU A 482 0 17.021 61.746 16.141 1.00 34.62                     ATOM 3674 OE2 GLU A 482 0 17.170 62.297 14.033 1.00 37.13                     ATOM 3675 N TRP A 483 0 13.311 60.124 18.857 1.00 25.91                       ATOM 3676 CA TRP A 483 0 12.496 59.280 19.711 1.00 25.49                      ATOM 3677 C TRP A 483 0 11.224 60.011 20.125 1.00 26.47                       ATOM 3678 O TRP A 483 0 10.155 59.405 20.116 1.00 26.95                       ATOM 3679 CB TRP A 483 0 13.216 58.807 20.974 1.00 21.98                      ATOM 3680 CG TRP A 483 0 12.376 58.144 22.013 1.00 21.49                      ATOM 3681 CD1 TRP A 483 0 11.960 56.827 22.003 1.00 20.81                     ATOM 3682 CD2 TRP A 483 0 11.818 58.730 23.194 1.00 20.14                     ATOM 3683 NE1 TRP A 483 0 11.187 56.575 23.143 1.00 20.29                     ATOM 3684 CE2 TRP A 483 0 11.097 57.736 23.868 1.00 20.29                     ATOM 3685 CE3 TRP A 483 0 11.875 60.006 23.754 1.00 21.32                     ATOM 3686 CZ2 TRP A 483 0 10.422 57.973 25.062 1.00 20.89                     ATOM 3687 CZ3 TRP A 483 0 11.217 60.248 24.946 1.00 20.78                     ATOM 3688 CH2 TRP A 483 0 10.495 59.227 25.596 1.00 21.44                     ATOM 3689 N ALA A 484 0 11.342 61.261 20.560 1.00 28.59                       ATOM 3690 CA ALA A 484 0 10.165 62.003 21.029 1.00 30.73                      ATOM 3691 C ALA A 484 0 9.226 62.350 19.869 1.00 30.42                        ATOM 3692 O ALA A 484 0 8.024 62.337 20.071 1.00 31.34                        ATOM 3693 CB ALA A 484 0 10.583 63.244 21.806 1.00 31.05                      ATOM 3694 N GLN A 485 0 9.702 62.488 18.653 1.00 30.79                        ATOM 3695 CA GLN A 485 0 8.927 62.742 17.466 1.00 33.16                       ATOM 3696 C GLN A 485 0 8.026 61.608 17.017 1.00 32.81                        ATOM 3697 O GLN A 485 0 7.044 61.847 16.302 1.00 32.74                        ATOM 3698 CB GLN A 485 0 9.859 63.113 16.290 1.00 34.56                       ATOM 3699 CG GLN A 485 0 10.631 64.361 16.686 1.00 39.67                      ATOM 3700 CD GLN A 485 0 11.559 64.919 15.640 1.00 42.86                      ATOM 3701 OE1 GLN A 485 0 11.528 66.145 15.434 1.00 45.48                     ATOM 3702 NE2 GLN A 485 0 12.375 64.103 14.982 1.00 44.07                     ATOM 3703 N LEU A 486 0 8.328 60.380 17.443 1.00 30.46                        ATOM 3704 CA LEU A 486 0 7.500 59.231 17.095 1.00 27.76                       ATOM 3705 C LEU A 486 0 6.051 59.510 17.509 1.00 28.23                        ATOM 3706 O LEU A 486 0 5.100 59.331 16.752 1.00 26.71                        ATOM 3707 CB LEU A 486 0 8.043 58.034 17.838 1.00 25.03                       ATOM 3708 CG LEU A 486 0 8.988 57.012 17.226 1.00 24.18                       ATOM 3709 CD1 LEU A 486 0 9.780 57.416 16.011 1.00 21.41                      ATOM 3710 CD2 LEU A 486 0 9.864 56.464 18.342 1.00 23.28                      ATOM 3711 N CYS A 487 0 5.870 59.974 18.739 1.00 28.05                        ATOM 3712 CA CYS A 487 0 4.560 60.263 19.279 1.00 30.77                       ATOM 3713 C CYS A 487 0 3.823 61.350 18.499 1.00 33.19                        ATOM 3714 O CYS A 487 0 2.627 61.170 18.263 1.00 33.69                        ATOM 3715 CB CYS A 487 0 4.643 60.637 20.752 1.00 27.94                       ATOM 3716 SG CYS A 487 0 5.214 59.280 21.781 1.00 27.23                       ATOM 3717 N GLU A 488 0 4.543 62.373 18.064 1.00 35.80                        ATOM 3718 CA GLU A 488 0 3.871 63.458 17.334 1.00 39.12                       ATOM 3719 C GLU A 488 0 3.384 62.928 15.995 1.00 37.78                        ATOM 3720 O GLU A 488 0 2.186 63.025 15.711 1.00 37.61                        ATOM 3721 CB GLU A 488 0 4.737 64.697 17.257 1.00 42.04                       ATOM 3722 CG GLU A 488 0 5.667 64.822 16.064 1.00 47.75                       ATOM 3723 CD GLU A 488 0 5.634 66.239 15.500 1.00 51.36                       ATOM 3724 OE1 GLU A 488 0 5.501 66.422 14.266 1.00 52.66                      ATOM 3725 OE2 GLU A 488 0 5.743 67.154 16.358 1.00 53.40                      ATOM 3726 N ILE A 489 0 4.263 62.253 15.267 1.00 36.63                        ATOM 3727 CA ILE A 489 0 3.906 61.647 14.004 1.00 36.74                       ATOM 3728 C ILE A 489 0 2.754 60.662 14.113 1.00 36.98                        ATOM 3729 O ILE A 489 0 1.847 60.664 13.276 1.00 38.60                        ATOM 3730 CB ILE A 489 0 5.089 60.903 13.361 1.00 36.57                       ATOM 3731 CG1 ILE A 489 0 6.267 61.853 13.148 1.00 36.46                      ATOM 3732 CG2 ILE A 489 0 4.651 60.305 12.030 1.00 36.90                      ATOM 3733 CD1 ILE A 489 0 7.535 61.194 12.654 1.00 35.62                      ATOM 3734 N TYR A 490 0 2.758 59.808 15.105 1.00 36.22                        ATOM 3735 CA TYR A 490 0 1.771 58.765 15.298 1.00 35.95                       ATOM 3736 C TYR A 490 0 0.413 59.314 15.692 1.00 37.83                        ATOM 3737 O TYR A 490 0 -0.581 58.816 15.165 1.00 39.24                       ATOM 3738 CB TYR A 490 0 2.206 57.817 16.409 1.00 32.47                       ATOM 3739 CG TYR A 490 0 1.314 56.641 16.663 1.00 30.55                       ATOM 3740 CD1 TYR A 490 0 1.176 55.623 15.726 1.00 29.96                      ATOM 3741 CD2 TYR A 490 0 0.610 56.536 17.849 1.00 29.79                      ATOM 3742 CE1 TYR A 490 0 0.378 54.528 15.975 1.00 29.51                      ATOM 3743 CE2 TYR A 490 0 -0.192 55.441 18.114 1.00 29.64                     ATOM 3744 CZ TYR A 490 0 -0.288 54.445 17.171 1.00 29.51                      ATOM 3745 OH TYR A 490 0 -1.101 53.363 17.437 1.00 32.06                      ATOM 3746 N ASP A 491 0 0.369 60.302 16.564 1.00 40.86                        ATOM 3747 CA ASP A 491 0 -0.909 60.887 16.963 1.00 43.97                      ATOM 3748 C ASP A 491 0 -1.586 61.633 15.811 1.00 45.30                       ATOM 3749 O ASP A 491 0 -2.809 61.752 15.820 1.00 45.60                       ATOM 3750 CB ASP A 491 0 -0.764 61.800 18.170 1.00 44.67                      ATOM 3751 CG ASP A 491 0 -0.441 61.101 19.475 1.00 45.90                      ATOM 3752 OD1 ASP A 491 0 0.149 61.761 20.364 1.00 46.32                      ATOM 3753 OD2 ASP A 491 0 -0.763 59.911 19.669 1.00 46.04                     ATOM 3754 N ASP A 492 0 -0.871 62.107 14.817 1.00 46.75                       ATOM 3755 CA ASP A 492 0 -1.323 62.804 13.653 1.00 48.98                      ATOM 3756 C ASP A 492 0 -1.702 61.936 12.460 1.00 49.48                       ATOM 3757 O ASP A 492 0 -2.002 62.458 11.378 1.00 50.24                       ATOM 3758 CB ASP A 492 0 -0.155 63.649 13.107 1.00 51.54                      ATOM 3759 CG ASP A 492 0 -0.168 65.081 13.587 1.00 53.57                      ATOM 3760 OD1 ASP A 492 0 -0.886 65.375 14.570 1.00 54.07                     ATOM 3761 OD2 ASP A 492 0 0.576 65.857 12.939 1.00 55.04                      ATOM 3762 N LEU A 493 0 -1.554 60.630 12.584 1.00 49.01                       ATOM 3763 CA LEU A 493 0 -1.896 59.732 11.483 1.00 47.63                      ATOM 3764 C LEU A 493 0 -3.377 59.872 11.137 1.00 47.61                       ATOM 3765 O LEU A 493 0 -4.209 60.018 12.027 1.00 47.02                       ATOM 3766 CB LEU A 493 0 -1.661 58.296 11.940 1.00 46.08                      ATOM 3767 CG LEU A 493 0 -0.485 57.463 11.464 1.00 45.24                      ATOM 3768 CD1 LEU A 493 0 0.616 58.224 10.756 1.00 43.57                      ATOM 3769 CD2 LEU A 493 0 0.075 56.710 12.669 1.00 44.62                      ATOM 3770 N PRO A 494 0 -3.694 59.763 9.866 1.00 48.01                        ATOM 3771 CA PRO A 494 0 -5.049 59.734 9*353 1.00 49.11                       ATOM 3772 C PRO A 494 0 -5.617 58.339 9.570 1.00 51.21                        ATOM 3773 O PRO A 494 0 -4.919 57.325 9.495 1.00 50.61                        ATOM 3774 CB PRO A 494 0 -4.938 59.995 7.843 1.00 48.94                       ATOM 3775 CG PRO A 494 0 -3.559 59.463 7.544 1.00 48.47                       ATOM 3776 CD PRO A 494 0 -2.714 59.538 8.797 1.00 48.22                       ATOM 3777 N PRO A 495 0 -6.915 58.238 9.796 1.00 53.24                        ATOM 3778 CA PRO A 495 0 -7.630 57.006 10.055 1.00 53.93                      ATOM 3779 C PRO A 495 0 -7.404 55.890 9.058 1.00 54.84                        ATOM 3780 O PRO A 495 0 -7.348 54.705 9.423 1.00 55.08                        ATOM 3781 CB PRO A 495 0 -9.126 57.362 10.146 1.00 54.40                      ATOM 3782 CG PRO A 495 0 -9.090 58.848 10.391 1.00 54.17                      ATOM 3783 CD PRO A 495 0 -7.787 59.420 9.895 1.00 53.58                       ATOM 3784 N GLU A 496 0 -7.190 56.198 7.784 1.00 55.36                        ATOM 3785 CA GLU A 496 0 -6.936 55.187 6.763 1.00 55.83                       ATOM 3786 C GLU A 496 0 -5.582 54.521 6.971 1.00 54.09                        ATOM 3787 O GLU A 496 0 -5.345 53.406 6.505 1.00 53.29                        ATOM 3788 CB GLU A 496 0 -7.091 55.805 5.378 1.00 57.96                       ATOM 3789 CG GLU A 496 0 -6.030 55.604 4.339 1.00 61.30                       ATOM 3790 CD GLU A 496 0 -6.448 54.984 3.025 1.00 63.68                       ATOM 3791 OE1 GLU A 496 0 -7.449 55.411 2.388 1.00 65.15                      ATOM 3792 OE2 GLU A 496 0 -5.747 54.034 2.586 1.00 64.91                      ATOM 3793 N ALA A 497 0 -4.665 55.217 7.630 1.00 52.35                        ATOM 3794 CA ALA A 497 0 -3.326 54.738 7.886 1.00 50.83                       ATOM 3795 C ALA A 497 0 -3.245 53.626 8.924 1.00 49.08                        ATOM 3796 O ALA A 497 0 -2.361 52.773 8.794 1.00 47.61                        ATOM 3797 CB ALA A 497 0 -2.443 55.910 8.317 1.00 51.23                       ATOM 3798 N THR A 498 0 -4.113 53.630 9.926 1.00 48.01                        ATOM 3799 CA THR A 498 0 -4.086 52.617 10.964 1.00 48.73                      ATOM 3800 C THR A 498 0 -5.271 51.656 10.938 1.00 48.99                       ATOM 3801 O THR A 498 0 -5.425 50.852 11.862 1.00 47.81                       ATOM 3802 CB THR A 498 0 -4.055 53.223 12.388 1.00 49.04                      ATOM 3803 OG1 THR A 498 0 -5.315 53.816 12.752 1.00 47.95                     ATOM 3804 CG2 THR A 498 0 -2.919 54.223 12.514 1.00 48.94                     ATOM 3805 N SER A 499 0 -6.101 51.756 9.911 1.00 49.78                        ATOM 3806 CA SER A 499 0 -7.307 50.933 9.814 1.00 51.20                       ATOM 3807 C SER A 499 0 -7.048 49.470 9.494 1.00 49.98                        ATOM 3808 O SER A 499 0 -6.257 49.143 8.617 1.00 48.80                        ATOM 3809 CB SER A 499 0 -8.223 51.606 8.800 1.00 52.62                       ATOM 3810 OG SER A 499 0 -8.428 50.827 7.596 1.00 55.22                       ATOM 3811 N ILE A 500 0 -7.706 48.585 10.230 1.00 50.08                       ATOM 3812 CA ILE A 500 0 -7.563 47.151 10.077 1.00 51.25                      ATOM 3813 C ILE A 500 0 -8.642 46.518 9.207 1.00 53.08                        ATOM 3814 O ILE A 500 0 -9.785 46.351 9.639 1.00 54.00                        ATOM 3815 CB ILE A 500 0 -7.631 46.428 11.436 1.00 50.61                      ATOM 3816 CG1 ILE A 500 0 -6.475 46.866 12.336 1.00 50.22                     ATOM 3817 CG2 ILE A 500 0 -7.619 44.907 11.302 1.00 50.34                     ATOM 3818 CD1 ILE A 500 0 -6.806 46.617 13.800 1.00 50.52                     ATOM 3819 N GLN A 501 0 -8.263 46.074 8.024 1.00 54.35                        ATOM 3820 CA GLN A 501 0 -9.177 45.360 7.129 1.00 55.14                       ATOM 3821 C GLN A 501 0 -9.298 43.904 7.564 1.00 55.85                        ATOM 3822 O GLN A 501 0 -8.335 43.130 7.556 1.00 55.59                        ATOM 3823 CB GLN A 501 0 -8.594 45.485 5.732 1.00 55.56                       ATOM 3824 CG GLN A 501 0 -9.262 44.736 4.604 1.00 56.32                       ATOM 3825 CD GLN A 501 0 -8.874 45.369 3.271 1.00 57.46                       ATOM 3826 OE1 GLN A 501 0 -8.480 44.667 2.336 1.00 57.35                      ATOM 3827 NE2 GLN A 501 0 -8.998 46.697 3.219 1.00 57.61                      ATOM 3828 N THR A 502 0 -10.493 43.506 7.968 1.00 57.08                       ATOM 3829 CA THR A 502 0 -10.788 42.146 8.401 1.00 58.28                      ATOM 3830 C THR A 502 0 -10.966 41.205 7.216 1.00 58.80                       ATOM 3831 O THR A 502 0 -11.199 41.604 6.074 1.00 58.71                       ATOM 3832 CB THR A 502 0 -12.046 42.108 9.293 1.00 58.99                      ATOM 3833 OG1 THR A 502 0 -11.794 42.909 10.464 1.00 59.62                    ATOM 3834 CG2 THR A 502 0 -12.421 40.707 9.749 1.00 58.74                     ATOM 3835 N VAL A 503 0 -10.746 39.922 7.471 1.00 59.20                       ATOM 3836 CA VAL A 503 0 -10.904 38.877 6.468 1.00 60.27                      ATOM 3837 C VAL A 503 0 -11.687 37.736 7.119 1.00 61.11                       ATOM 3838 O VAL A 503 0 -11.606 37.563 8.341 1.00 61.03                       ATOM 3839 CB VAL A 503 0 -9.589 38.430 5.823 1.00 59.97                       ATOM 3840 CG1 VAL A 503 0 -8.337 38.964 6.507 1.00 59.65                      ATOM 3841 CG2 VAL A 503 0 -9.467 36.914 5.722 1.00 59.97                      ATOM 3842 N VAL A 504 0 -12.478 37.002 6.341 1.00 61.77                       ATOM 3843 CA VAL A 504 0 -13.203 35.863 6.911 1.00 62.40                      ATOM 3844 C VAL A 504 0 -12.673 34.579 6.259 1.00 62.99                       ATOM 3845 O VAL A 504 0 -11.811 33.894 6.803 1.00 63.13                       ATOM 3846 CB VAL A 504 0 -14.730 35.882 6.756 1.00 62.39                      ATOM 3847 CG1 VAL A 504 0 -15.392 36.931 7.635 1.00 61.89                     ATOM 3848 CG2 VAL A 504 0 -15.127 36.068 5.297 1.00 62.17                     ATOM 3849 C1 NAG A 800 0 -2.401 42.835 45.802 1.00 30.44                      ATOM 3850 C2 NAG A 800 0 -1.327 43.232 46.780 1.00 31.80                      ATOM 3851 N2 NAG A 800 0 -0.119 43.561 45.983 1.00 31.37                      ATOM 3852 C7 NAG A 800 0 0.179 44.844 45.683 1.00 32.37                       ATOM 3853 O7 NAG A 800 0 -0.549 45.688 45.982 1.00 34.61                      ATOM 3854 C8 NAG A 800 0 1.457 45.094 44.983 1.00 31.67                       ATOM 3855 C3 NAG A 800 0 -1.015 42.187 47.801 1.00 32.94                      ATOM 3856 O3 NAG A 800 0 -0.264 42.838 48.796 1.00 34.46                      ATOM 3857 C4 NAG A 800 0 -2.351 41.662 48.377 1.00 34.05                      ATOM 3858 O4 NAG A 800 0 -2.097 40.644 49.344 1.00 35.62                      ATOM 3859 C5 NAG A 800 0 -3.128 41.025 47.202 1.00 35.11                      ATOM 3860 O5 NAG A 800 0 -3.466 42.046 46.295 1.00 33.06                      ATOM 3861 C6 NAG A 800 0 -4.444 40.420 47.673 1.00 36.66                      ATOM 3862 O6 NAG A 800 0 -5.199 41.411 48.288 1.00 39.73                      ATOM 3863 C1 GLC A 900 0 -8.957 50.280 6.333 1.00 58.53                       ATOM 3864 C2 GLC A 900 0 -8.500 49.605 5.037 1.00 59.25                       ATOM 3865 C3 GLC A 900 0 -7.806 50.686 4.219 1.00 59.71                       ATOM 3866 C4 GLC A 900 0 -8.691 51.905 3.987 1.00 60.13                       ATOM 3867 CS GLC A 900 0 -9.595 52.289 5.142 1.00 59.22                       ATOM 3868 O5 GLC A 900 0 -10.004 51.177 5.937 1.00 59.71                      ATOM 3869 CU IUM B 1 0 -1.332 34.401 30.132 1.00 29.47                        ATOM 3870 CU IUM B 2 0 7.297 42.245 26.618 1.00 27.01                         ATOM 3871 CU IUM B 3 0 9.569 38.786 23.923 1.00 21.38                         ATOM 3872 O IUM B 5 0 7.445 40.703 25.162 1.00 26.99                          ATOM 3873 OWO WAT W 1 0 19.509 36.893 30.054 1.00 13.07                       ATOM 3874 OWO WAT W 2 0 24.726 29.672 16.651 1.00 7.67                        ATOM 3875 OWO WAT W 3 0 15.295 17.988 35.061 1.00 8.65                        ATOM 3876 OWO WAT W 4 0 6.481 28.311 23.427 1.00 8.00                         ATOM 3877 OWO WAT W 5 0 14.921 45.178 24.306 1.00 17.04                       ATOM 3878 OWO WAT W 6 0 14.413 44.401 28.162 1.00 10.12                       ATOM 3879 OWO WAT W 7 0 9.967 21.576 9.620 1.00 11.43                         ATOM 3880 OWO WAT W 8 0 10.088 28.675 13.038 1.00 9.27                        ATOM 3881 OWO WAT W 9 0 9.808 47.902 28.959 1.00 12.71                        ATOM 3882 OWO WAT W 10 0 21.976 23.052 35.604 1.00 11.72                      ATOM 3883 OWO WAT W 11 0 10.862 25.744 29.928 1.00 10.21                      ATOM 3884 OWO WAT W 12 0 26.087 32.996 23.097 1.00 14.21                      ATOM 3885 OWO WAT W 13 0 22.256 58.745 37.931 1.00 17.85                      ATOM 3886 OWO WAT W 14 0 -0.104 29.831 35.249 1.00 16.36                      ATOM 3887 OWO WAT W 15 0 18.153 61.857 36.641 1.00 14.38                      ATOM 3888 OWO WAT W 16 0 9.426 38.431 9.161 1.00 15.35                        ATOM 3889 OWO WAT W 17 0 7.639 24.371 3.713 1.00 22.18                        ATOM 3890 OWO WAT W 18 0 27.977 11.643 9.481 1.00 19.22                       ATOM 3891 OWO WAT W 19 0 3.140 21.028 24.695 1.00 11.12                       ATOM 3892 OWO WAT W 20 0 9.847 20.701 30.902 1.00 16.16                       ATOM 3893 OWO WAT W 21 0 -1.517 29.009 43.180 1.00 27.18                      ATOM 3894 OWO WAT W 22 0 3.497 29.138 26.088 1.00 17.2                        ATOM 3895 OWO WAT W 23 0 20.614 32.765 40.433 1.00 17.63                      ATOM 3896 OWO WAT W 24 0 19.098 51.778 39.452 1.00 22.33                      ATOM 3897 OWO WAT W 25 0 0.977 21.396 5.064 1.00 18.54                        ATOM 3898 OWO WAT W 26 0 8.546 16.150 21.761 1.00 16.40                       ATOM 3899 OWO WAT W 27 0 6.102 19.858 10.350 1.00 17.79                       ATOM 3900 OWO WAT W 28 0 11.702 55.189 41.955 1.00 18.92                      ATOM 3901 OWO WAT W 29 0 3.360 42.251 18.209 1.00 16.26                       ATOM 3902 OWO WAT W 30 0 6.232 14.672 22.473 1.00 24.49                       ATOM 3903 OWO WAT W 31 0 16.729 26.542 39.731 1.00 15.28                      ATOM 3904 OWO WAT W 32 0 2.834 30.640 40.601 1.00 18.11                       ATOM 3905 OWO WAT W 33 0 21.893 42.837 27.884 1.00 15.08                      ATOM 3906 OWO WAT W 34 0 1.581 28.193 27.914 1.00 17.77                       ATOM 3907 OWO WAT W 35 0 -3.503 21.749 11.578 1.00 15.32                      ATOM 3908 OWO WAT W 36 0 7.131 33.344 11.786 1.00 18.18                       ATOM 3909 OWO WAT W 37 0 17.312 38.603 29.961 1.00 14.75                      ATOM 3910 OWO WAT W 38 0 -6.705 40.723 39.909 1.00 23.49                      ATOM 3911 OWO WAT W 39 0 9.010 31.121 11.736 1.00 19.99                       ATOM 3912 OWO WAT W 40 0 9.376 28.353 33.076 1.00 16.22                       ATOM 3913 OWO WAT W 41 0 30.104 29.895 20.857 1.00 25.77                      ATOM 3914 OWO WAT W 42 0 -6.950 33.663 21.335 1.00 26.62                      ATOM 3915 OWO WAT W 43 0 8.541 27.867 36.827 1.00 12.80                       ATOM 3916 OWO WAT W 44 0 3.590 21.651 11.893 1.00 14.46                       ATOM 3917 OWO WAT W 45 0 23.290 21.665 37.787 1.00 28.75                      ATOM 3918 OWO WAT W 46 0 22.724 11.873 22.270 1.00 23.07                      ATOM 3919 OWO WAT W 47 0 -1.090 42.001 12.877 1.00 19.33                      ATOM 3920 OWO WAT W 48 0 14.091 27.298 40.583 1.00 18.51                      ATOM 3921 OWO WAT W 49 0 2.336 52.026 29.983 1.00 25.66                       ATOM 3922 OWO WAT W 50 0 15.475 14.450 22.853 1.00 20.37                      ATOM 3923 OWO WAT W 51 0 25.945 26.568 40.287 1.00 24.49                      ATOM 3924 OWO WAT W 52 0 19.545 41.598 35.087 1.00 20.70                      ATOM 3925 OWO WAT W 53 0 -3.802 47.942 9.638 1.00 29.98                       ATOM 3926 OWO WAT W 54 0 -7.478 41.160 9.585 1.00 24.26                       ATOM 3927 OWO WAT W 55 0 -2.938 29.733 36.048 1.00 22.93                      ATOM 3928 OWO WAT W 56 0 29.051 32.114 22.680 1.00 22.50                      ATOM 3929 OWO WAT W 57 0 0.360 29.505 5.595 1.00 17.78                        ATOM 3930 OWO WAT W 58 0 8.583 57.422 21.440 1.00 21.90                       ATOM 3931 OWO WAT W 59 0 25.151 31.947 34.812 1.00 22.13                      ATOM 3932 OWO WAT W 60 0 25.133 62.204 32.968 1.00 25.75                      ATOM 3933 OWO WAT W 61 0 14.909 40.770 30.294 1.00 17.25                      ATOM 3934 OWO WAT W 62 0 20.825 30.520 34.676 1.00 16.18                      ATOM 3935 OWO WAT W 63 0 5.509 26.744 43.167 1.00 30.12                       ATOM 3936 OWO WAT W 64 0 5.280 57.279 14.627 1.00 22.66                       ATOM 3937 OWO WAT W 65 0 2.944 53.436 32.359 1.00 22.97                       ATOM 3938 OWO WAT W 66 0 11.266 43.508 3.407 1.00 20.01                       ATOM 3939 OWO WAT W 67 0 21.535 45.549 26.563 1.00 24.47                      ATOM 3940 OWO WAT W 68 0 0.412 33.358 11.837 1.00 19.89                       ATOM 3941 OWO WAT W 69 0 26.466 32.305 25.785 1.00 20.19                      ATOM 3942 OWO WAT W 70 0 0.910 45.068 7.829 1.00 22.05                        ATOM 3943 OWO WAT W 71 0 -2.060 46.506 39.381 1.00 23.49                      ATOM 3944 OWO WAT W 72 0 20.236 56.718 25.851 1.00 23.74                      ATOM 3945 OWO WAT W 73 0 3.253 23.017 38.254 1.00 24.83                       ATOM 3946 OWO WAT W 74 0 9.653 22.835 35.143 1.00 25.79                       ATOM 3947 OWO WAT W 75 0 16.877 52.904 47.331 1.00 24.42                      ATOM 3948 OWO WAT W 76 0 14.293 22.021 3.993 1.00 32.28                       ATOM 3949 OWO WAT W 77 0 -5.287 19.835 18.528 1.00 24.65                      ATOM 3950 OWO WAT W 78 0 8.414 38.317 49.069 1.00 28.77                       ATOM 3951 OWO WAT W 79 0 7.070 32.466 47.926 1.00 21.83                       ATOM 3952 OWO WAT W 80 0 -0.452 28.307 25.779 1.00 16.58                      ATOM 3953 OWO WAT W 81 0 14.774 15.006 34.455 1.00 25.63                      ATOM 3954 OWO WAT W 82 0 11.515 54.942 35.962 1.00 14.20                      ATOM 3955 OWO WAT W 83 0 25.643 33.451 32.105 1.00 30.31                      ATOM 3956 OWO WAT W 84 0 11.869 12.221 20.394 1.00 31.37                      ATOM 3957 OWO WAT W 85 0 11.653 51.587 22.411 1.00 16.48                      ATOM 3958 OWO WAT W 86 0 17.334 40.837 51.079 1.00 30.26                      ATOM 3959 OWO WAT W 87 0 4.355 25.208 34.030 1.00 32.26                       ATOM 3960 OWO WAT W 88 0 18.816 52.360 32.512 1.00 21.19                      ATOM 3961 OWO WAT W 89 0 -2.704 46.518 35.364 1.00 21.99                      ATOM 3962 OWO WAT W 90 0 18.793 27.893 49.481 1.00 24.52                      ATOM 3963 OWO WAT W 91 0 22.459 46.584 28.898 1.00 18.99                      ATOM 3964 OWO WAT W 92 0 7.958 34.422 49.370 1.00 26.14                       ATOM 3965 OWO WAT W 93 0 23.972 16.246 6.806 1.00 24.35                       ATOM 3966 OWO WAT W 94 0 1.340 49.185 26.307 1.00 31.64                       ATOM 3967 OWO WAT W 95 0 -1.830 35.291 12.266 1.00 27.28                      ATOM 3968 OWO WAT W 96 0 20.460 17.486 3.589 1.00 33.51                       ATOM 3969 OWO WAT W 97 0 15.177 6.964 9.868 1.00 24.40                        ATOM 3970 OWO WAT W 98 0 18.616 57.927 43.922 1.00 30.76                      ATOM 3971 OWO WAT W 99 0 10.562 32.112 9.972 1.00 28.90                       ATOM 3972 OWO WAT W 100 0 1.630 61.363 10.878 1.00 33.92                      ATOM 3973 OWO WAT W 101 0 -4.939 49.989 33.211 1.00 29.73                     ATOM 3974 OWO WAT W 102 0 19.385 44.813 34.546 1.00 23.52                     ATOM 3975 OWO WAT W 103 0 19.055 43.063 37.581 1.00 30.59                     ATOM 3976 OWO WAT W 105 0 28.703 33.555 27.406 1.00 32.92                     ATOM 3977 OWO WAT W 106 0 28.835 19.646 10.759 1.00 40.44                     ATOM 3978 OWO WAT W 107 0 22.047 22.465 9.758 1.00 29.98                      ATOM 3979 OWO WAT W 108 0 14.689 61.032 36.346 1.00 30.63                     ATOM 3980 OWO WAT W 109 0 16.998 24.042 9.318 1.00 23.90                      ATOM 3981 OWO WAT W 110 0 13.472 30.533 11.848 1.00 34.83                     ATOM 3982 OWO WAT W 111 0 -2.175 35.601 41.496 1.00 28.55                     ATOM 3983 OWO WAT W 112 0 1.528 17.373 -1.396 1.00 38.21                      ATOM 3984 OWO WAT W 113 0 -2.856 29.748 19.681 1.00 30.55                     ATOM 3985 OWO WAT W 114 0 2.377 42.810 47.971 1.00 26.87                      ATOM 3986 OWO WAT W 115 0 10.947 12.820 33.745 1.00 31.60                     ATOM 3987 OWO WAT W 116 0 9.807 58.194 12.442 1.00 29.63                      ATOM 3988 OWO WAT W 117 0 18.488 62.559 29.470 1.00 45.83                     ATOM 3989 OWO WAT W 118 0 11.708 61.566 40.940 1.00 37.19                     ATOM 3990 OWO WAT W 119 0 -10.101 22.257 15.091 1.00 30.48                    ATOM 3991 OWO WAT W 120 0 -1.930 15.913 7.386 1.00 36.63                      ATOM 3992 OWO WAT W 121 0 23.988 43.686 29.319 1.00 32.15                     ATOM 3993 OWO WAT W 122 0 7.354 57.153 12.809 1.00 28.10                      ATOM 3994 OWO WAT W 123 0 24.207 22.101 11.958 1.00 32.83                     ATOM 3995 OWO WAT W 124 0 -1.268 15.083 9.738 1.00 32.53                      ATOM 3996 OWO WAT W 125 0 19.363 5.047 13.812 1.00 34.57                      ATOM 3997 OWO WAT W 126 0 4.799 41.145 23.688 1.00 28.33                      ATOM 3998 OWO WAT W 127 0 15.975 23.287 5.889 1.00 30.95                      ATOM 3999 OWO WAT W 128 0 3.698 38.582 -2.369 1.00 36.84                      ATOM 4000 OWO WAT W 129 0 -2.601 49.124 11.710 1.00 28.91                     ATOM 4001 OWO WAT W 130 0 15.779 56.598 43.285 1.00 27.76                     ATOM 4002 OWO WAT W 131 0 26.306 32.724 13.233 1.00 37.94                     ATOM 4003 OWO WAT W 132 0 3.610 46.947 23.991 1.00 35.49                      ATOM 4004 OWO WAT W 133 0 18.354 11.929 29.348 1.00 33.88                     ATOM 4005 OWO WAT W 134 0 13.966 41.517 27.765 1.00 18.02                     ATOM 4006 OWO WAT W 135 0 23.545 49.080 27.785 1.00 25.21                     ATOM 4007 OWO WAT W 136 0 16.876 25.082 41.791 1.00 28.71                     ATOM 4008 OWO WAT W 137 0 15.439 54.809 45.527 1.00 35.30                     ATOM 4009 OWO WAT W 138 0 11.733 25.676 43.264 1.00 38.24                     ATOM 4010 OWO WAT W 139 0 9.795 34.460 11.898 1.00 31.61                      ATOM 4011 OWO WAT W 140 0 13.328 57.569 42.356 1.00 30.66                     ATOM 4012 OWO WAT W 141 0 14.146 7.869 20.604 1.00 35.72                      ATOM 4013 OWO WAT W 142 0 23.330 12.948 3.922 1.00 29.83                      ATOM 4014 OWO WAT W 143 0 16.607 10.575 24.347 1.00 36.47                     ATOM 4015 OWO WAT W 144 0 8.509 25.546 35.012 1.00 35.43                      ATOM 4016 OWO WAT W 145 0 12.597 44.457 1.450 1.00 39.54                      ATOM 4017 OWO WAT W 146 0 21.680 51.509 39.154 1.00 40.08                     ATOM 4018 OWO WAT W 147 0 -0.702 52.593 39.700 1.00 29.62                     ATOM 4019 OWO WAT W 148 0 23.269 14.719 22.589 1.00 30.24                     ATOM 4020 OWO WAT W 149 0 27.149 22.972 41.846 1.00 35.00                     ATOM 4021 OWO WAT W 150 0 2.854 9.792 8.923 1.00 46.35                        ATOM 4022 OWO WAT W 151 0 24.831 15.672 24.889 1.00 29.22                     ATOM 4023 OWO WAT W 152 0 24.965 51.606 19.113 1.00 32.19                     ATOM 4024 OWO WAT W 153 0 -4.611 25.034 37.817 1.00 46.51                     ATOM 4025 OWO WAT W 154 0 12.225 39.382 28.864 1.00 25.42                     ATOM 4026 OWO WAT W 155 0 18.332 22.341 43.180 1.00 36.18                     ATOM 4027 OWO WAT W 156 0 36.467 20.701 17.144 1.00 44.13                     ATOM 4028 OWO WAT W 157 0 -4.903 47.901 40.886 1.00 33.97                     ATOM 4029 OWO WAT W 158 0 12.979 13.955 3.208 1.00 33.60                      ATOM 4030 OWO WAT W 159 0 32.383 12.693 24.743 1.00 30.25                     ATOM 4031 OWO WAT W 160 0 30.796 26.296 14.368 1.00 44.37                     ATOM 4032 OWO WAT W 161 0 19.332 37.280 40.057 1.00 31.54                     ATOM 4033 OWO WAT W 162 0 17.625 20.028 41.642 1.00 45.88                     ATOM 4034 OWO WAT W 163 0 19.917 56.115 46.103 1.00 40.37                     ATOM 4035 OWO WAT W 164 0 -4.743 14.204 16.748 1.00 40.86                     ATOM 4036 OWO WAT W 165 0 0.738 46.912 21.790 1.00 38.56                      ATOM 4037 OWO WAT W 166 0 22.648 62.277 30.976 1.00 24.37                     ATOM 4038 OWO WAT W 167 0 -4.322 45.754 26.894 1.00 48.97                     ATOM 4039 OWO WAT W 168 0 -2.386 24.601 0.665 1.00 32.57                      ATOM 4040 OWO WAT W 169 0 -0.459 41.618 35.838 1.00 35.25                     ATOM 4041 OWO WAT W 170 0 26.659 4.722 11.434 1.00 41.25                      ATOM 4042 OWO WAT W 171 0 13.720 11.379 22.121 1.00 39.59                     ATOM 4043 OWO WAT W 172 0 15.266 7.451 6.576 1.00 41.71                       ATOM 4044 OWO WAT W 173 0 0.134 17.450 6.165 1.00 42.12                       ATOM 4045 OWO WAT W 174 0 38.646 32.884 25.247 1.00 41.80                     ATOM 4046 OWO WAT W 175 0 10.591 17.398 3.251 1.00 29.37                      ATOM 4047 OWO WAT W 176 0 22.444 49.424 25.264 1.00 19.51                     ATOM 4048 OWO WAT W 177 0 0.429 23.224 28.598 1.00 33.54                      ATOM 4049 OWO WAT W 178 0 -2.302 27.278 34.780 1.00 44.76                     ATOM 4050 OWO WAT W 179 0 2.054 25.866 16.462 1.00 34.29                      ATOM 4051 OWO WAT W 180 0 30.277 18.006 25.789 1.00 42.28                     ATOM 4052 OWO WAT W 181 0 2.316 18.424 27.884 1.00 47.39                      ATOM 4053 OWO WAT W 182 0 19.401 41.164 39.560 1.00 39.68                     ATOM 4054 OWO WAT W 183 0 23.742 10.982 24.879 1.00 43.32                     ATOM 4055 OWO WAT W 184 0 3.926 24.450 44.251 1.00 48.95                      ATOM 4056 OWO WAT W 185 0 25.186 21.211 40.951 1.00 39.05                     ATOM 4057 OWO WAT W 186 0 20.353 34.816 48.799 1.00 34.08                     ATOM 4058 OWO WAT W 187 0 35.782 22.476 21.693 1.00 40.04                     ATOM 4059 OWO WAT W 188 0 27.256 23.617 12.235 1.00 40.85                     ATOM 4060 OWO WAT W 189 0 6.777 12.502 12.641 1.00 53.37                      ATOM 4061 OWO WAT W 190 0 -4.663 38.998 4.159 1.00 39.85                      ATOM 4062 OWO WAT W 191 0 24.398 52.064 24.607 1.00 45.51                     ATOM 4063 OWO WAT W 192 0 1.808 15.541 4.832 1.00 41.06                       ATOM 4064 OWO WAT W 193 0 5.341 36.359 7.569 1.00 39.36                       ATOM 4065 OWO WAT W 194 0 32.192 38.650 21.799 1.00 37.18                     ATOM 4066 OWO WAT W 195 0 -10.782 36.616 38.705 1.00 50.35                    ATOM 4067 OWO WAT W 196 0 4.119 64.116 32.946 1.00 34.51                      ATOM 4068 OWO WAT W 197 0 19.427 22.772 5.898 1.00 37.94                      ATOM 4069 OWO WAT W 198 0 -4.671 33.476 1.652 1.00 43.38                      ATOM 4070 OWO WAT W 199 0 -8.983 23.757 17.693 1.00 57.10                     ATOM 4071 OWO WAT W 200 0 -6.735 22.473 20.432 1.00 38.49                     ATOM 4072 OWO WAT W 201 0 -6.954 26.746 37.309 1.00 55.48                     ATOM 4073 OWO WAT W 202 0 23.418 38.662 33.700 1.00 42.20                     ATOM 4074 OWO WAT W 203 0 9.004 24.070 36.971 1.00 40.06                      ATOM 4075 OWO WAT W 204 0 18.890 42.920 51.502 1.00 46.29                     ATOM 4076 OWO WAT W 205 0 13.301 18.514 3.624 1.00 42.17                      ATOM 4077 OWO WAT W 206 0 31.189 12.995 19.645 1.00 51.92                     ATOM 4078 OWO WAT W 207 0 15.589 57.456 13.738 1.00 38.96                     ATOM 4079 OWO WAT W 208 0 -3.389 12.961 12.738 1.00 46.99                     ATOM 4080 OWO WAT W 209 0 9.321 30.475 6.320 1.00 49.75                       ATOM 4081 OWO WAT W 210 0 1.680 61.379 33.738 1.00 37.48                      ATOM 4082 OWO WAT W 211 0 -3.811 36.417 3.807 1.00 46.01                      ATOM 4083 OWO WAT W 212 0 17.087 46.902 3.830 1.00 45.12                      ATOM 4084 OWO WAT W 213 0 23.702 22.325 43.022 1.00 36.14                     ATOM 4085 OWO WAT W 214 0 10.849 60.003 14.389 1.00 32.05                     ATOM 4086 OWO WAT W 215 0 34.001 25.493 20.855 1.00 40.75                     ATOM 4087 OWO WAT W 216 0 27.422 37.093 28.951 1.00 42.33                     ATOM 4088 OWO WAT W 217 0 2.471 63.256 35.173 1.00 48.36                      ATOM 4089 OWO WAT W 218 0 -0.973 59.086 28.720 1.00 53.14                     ATOM 4090 OWO WAT W 219 0 28.841 9.287 6.463 1.00 39.02                       ATOM 4091 OWO WAT W 220 0 -5.593 21.802 9.619 1.00 44.21                      ATOM 4092 OWO WAT W 221 0 22.109 15.521 1.696 1.00 38.33                      ATOM 4093 OWO WAT W 222 0 13.029 32.860 12.233 1.00 37.63                     ATOM 4094 OWO WAT W 223 0 11.840 33.823 3.800 1.00 42.20                      ATOM 4095 OWO WAT W 224 0 8.476 42.976 -0.104 1.00 40.23                      ATOM 4096 OWO WAT W 225 0 6.607 9.754 13.906 1.00 41.30                       ATOM 4097 OWO WAT W 226 0 22.513 32.613 49.067 1.00 47.26                     ATOM 4098 OWO WAT W 227 0 13.790 4.924 16.718 1.00 38.05                      ATOM 4099 OWO WAT W 228 0 4.578 46.381 2.146 1.00 38.90                       ATOM 4100 OWO WAT W 229 0 -0.178 18.054 23.533 1.00 43.42                     ATOM 4101 OWO WAT W 230 0 -5.146 34.010 4.766 1.00 38.90                      ATOM 4102 OWO WAT W 231 0 20.232 28.890 51.507 1.00 44.95                     ATOM 4103 OWO WAT W 232 0 16.083 32.879 10.309 1.00 45.29                     ATOM 4104 OWO WAT W 233 0 22.111 51.333 10.599 1.00 34.03                     ATOM 4105 OWO WAT W 234 0 3.247 15.790 28.046 1.00 50.25                      ATOM 4106 OWO WAT W 235 0 5.547 11.598 9.674 1.00 56.39                       ATOM 4107 OWO WAT W 236 0 -1.085 18.297 -2.265 1.00 45.26                     ATOM 4108 OWO WAT W 237 0 30.994 12.013 22.690 1.00 50.37                     ATOM 4109 OWO WAT W 238 0 24.691 33.260 27.819 1.00 37.65                     ATOM 4110 OWO WAT W 239 0 18.911 40.770 5.815 1.00 44.15                      ATOM 4111 OWO WAT W 240 0 21.532 53.033 33.280 1.00 31.23                     ATOM 4112 OWO WAT W 241 0 19.745 46.029 4.364 1.00 46.38                      ATOM 4113 OWO WAT W 242 0 27.516 16.526 25.474 1.00 51.75                     ATOM 4114 OWO WAT W 243 0 34.171 19.604 8.423 1.00 55.79                      ATOM 4115 OWO WAT W 244 0 23.870 53.512 11.474 1.00 42.01                     ATOM 4116 OWO WAT W 245 0 14.492 23.842 44.882 1.00 52.25                     ATOM 4117 OWO WAT W 246 0 -3.070 63.260 33.189 1.00 40.77                     ATOM 4118 OWO WAT W 247 0 22.185 55.701 37.353 1.00 39.52                     ATOM 4119 OWO WAT W 248 0 14.144 26.239 42.825 1.00 42.50                     ATOM 4120 OWO WAT W 249 0 25.026 36.545 35.213 1.00 58.19                     ATOM 4121 OWO WAT W 250 0 27.072 34.293 43.895 1.00 46.58                     ATOM 4122 OWO WAT W 251 0 11.742 7.192 4.856 1.00 42.78                       ATOM 4123 OWO WAT W 252 0 0.730 46.405 24.947 1.00 39.31                      ATOM 4124 OWO WAT W 253 0 28.346 34.036 30.808 1.00 43.10                     ATOM 4125 OWO WAT W 254 0 -3.838 40.281 1.903 1.00 38.67                      ATOM 4126 OWO WAT W 255 0 6.837 35.163 51.935 1.00 58.57                      ATOM 4127 OWO WAT W 256 0 19.740 62.853 17.880 1.00 52.39                     ATOM 4128 OWO WAT W 258 0 -0.994 41.755 22.088 0.00 69.57                     ATOM 4129 OWO WAT W 259 0 1.221 10.473 15.458 1.00 54.80                      ATOM 4130 OWO WAT W 260 0 23.445 55.367 31.430 1.00 48.90                     ATOM 4131 OWO WAT W 261 0 23.757 57.854 34.657 1.00 37.69                     ATOM 4132 OWO WAT W 262 0 8.508 19.111 34.572 1.00 55.52                      ATOM 4133 OWO WAT W 263 0 22.806 22.381 3.611 1.00 64.20                      ATOM 4134 OWO WAT W 264 0 0.398 22.602 42.625 1.00 58.86                      ATOM 4135 OWO WAT W 265 0 4.195 52.287 43.465 1.00 36.84                      ATOM 4136 OWO WAT W 266 0 20.211 6.536 4.911 1.00 39.34                       ATOM 4137 OWO WAT W 267 0 14.680 16.117 2.803 1.00 45.76                      ATOM 4138 OWO WAT W 268 0 14.938 25.582 6.850 1.00 41.01                      ATOM 4139 OWO WAT W 269 0 7.763 7.940 31.891 0.00 71.30                       ATOM 4140 OWO WAT W 270 0 -3.459 33.491 39.400 1.00 40.80                     ATOM 4141 OWO WAT W 271 0 23.154 22.897 6.985 1.00 48.25                      ATOM 4142 OWO WAT W 272 0 34.916 25.555 28.092 1.00 52.63                     ATOM 4143 OWO WAT W 273 0 8.332 45.481 50.776 1.00 47.23                      ATOM 4144 OWO WAT W 274 0 -3.441 57.643 28.775 1.00 49.70                     ATOM 4145 OWO WAT W 275 0 23.213 40.573 47.561 1.00 56.02                     ATOM 4146 OWO WAT W 276 0 5.421 55.179 45.172 1.00 52.70                      ATOM 4147 OWO WAT W 277 0 -3.012 21.908 40.933 1.00 41.69                     ATOM 4148 OWO WAT W 278 0 26.328 53.637 17.905 1.00 37.80                     ATOM 4149 OWO WAT W 279 0 9.740 58.922 43.485 1.00 52.06                      ATOM 4150 OWO WAT W 280 0 23.545 15.660 4.258 1.00 41.55                      ATOM 4151 OWO WAT W 281 0 22.652 31.154 51.246 1.00 58.65                     ATOM 4152 OWO WAT W 282 0 22.192 51.135 8.251 1.00 44.76                      ATOM 4153 OWO WAT W 283 0 -6.046 22.886 24.288 1.00 52.40                     ATOM 4154 OWO WAT W 284 0 19.949 45.276 49.516 1.00 54.58                     ATOM 4155 OWO WAT W 285 0 7.388 22.308 32.108 1.00 43.62                      ATOM 4156 OWO WAT W 286 0 15.080 50.452 2.795 1.00 52.20                      ATOM 4157 OWO WAT W 287 0 1.016 62.235 30.878 1.00 56.81                      ATOM 4158 OWO WAT W 288 0 23.803 52.570 27.699 1.00 56.22                     ATOM 4159 OWO WAT W 289 0 -10.525 31.623 13.870 1.00 47.21                    ATOM 4160 OWO WAT W 290 0 1.599 55.502 24.567 1.00 44.50                      ATOM 4161 OWO WAT W 291 0 -15.671 37.251 14.660 1.00 83.62                    ATOM 4162 OWO WAT W 292 0 7.231 7.950 17.754 1.00 50.61                       ATOM 4163 OWO WAT W 293 0 -4.009 34.057 42.492 1.00 78.48                     ATOM 4164 OWO WAT W 294 0 21.004 58.371 18.690 1.00 61.15                     ATOM 4165 OWO WAT W 295 0 16.405 48.869 52.211 1.00 53.17                     ATOM 4166 OWO WAT W 296 0 7.329 31.202 1.964 1.00 38.86                       ATOM 4167 OWO WAT W 297 0 9.518 53.886 5.467 1.00 41.62                       ATOM 4168 OWO WAT W 298 0 10.398 48.995 0.335 1.00 49.64                      ATOM 4169 OWO WAT W 299 0 9.889 15.077 3.774 1.00 42.28                       ATOM 4170 OWO WAT W 300 0 15.854 56.731 10.934 1.00 44.02                   __________________________________________________________________________

    __________________________________________________________________________    #             SEQUENCE LISTING                                                   - -  - - (1) GENERAL INFORMATION:                                             - -    (iii) NUMBER OF SEQUENCES: 10                                          - -  - - (2) INFORMATION FOR SEQ ID NO: 1:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 539 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #1:                           - - Met Phe Lys Asn Leu Leu Ser Phe Ala Leu Le - #u Ala Ile Ser Val        Ala                                                                             1               5   - #                10  - #                15              - - Asn Ala Gln Ile Val Asn Ser Val Asp Thr Me - #t Thr Leu Thr Asn Ala                  20      - #            25      - #            30                   - - Asn Val Ser Pro Asp Gly Phe Thr Arg Ala Gl - #y Ile Leu Val Asn Gly              35          - #        40          - #        45                       - - Val His Gly Pro Leu Ile Arg Gly Gly Lys As - #n Asp Asn Phe Glu Leu          50              - #    55              - #    60                           - - Asn Val Val Asn Asp Leu Asp Asn Pro Thr Me - #t Leu Arg Pro Thr Ser      65                  - #70                  - #75                  - #80        - - Ile His Trp His Gly Leu Phe Gln Arg Gly Th - #r Asn Trp Ala Asp Gly                      85  - #                90  - #                95               - - Ala Asp Gly Val Asn Gln Cys Pro Ile Ser Pr - #o Gly His Ala Phe Leu                  100      - #           105      - #           110                  - - Tyr Lys Phe Thr Pro Ala Gly His Ala Gly Th - #r Phe Trp Tyr His Ser              115          - #       120          - #       125                      - - His Phe Gly Thr Gln Tyr Cys Asp Gly Leu Ar - #g Gly Pro Met Val Ile          130              - #   135              - #   140                          - - Tyr Asp Asp Asn Asp Pro His Ala Ala Leu Ty - #r Asp Glu Asp Asp Glu      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Asn Thr Ile Ile Thr Leu Ala Asp Trp Tyr Hi - #s Ile Pro Ala Pro        Ser                                                                                             165  - #               170  - #               175             - - Ile Gln Gly Ala Ala Gln Pro Asp Ala Thr Le - #u Ile Asn Gly Lys Gly                  180      - #           185      - #           190                  - - Arg Tyr Val Gly Gly Pro Ala Ala Glu Leu Se - #r Ile Val Asn Val Glu              195          - #       200          - #       205                      - - Gln Gly Lys Lys Tyr Arg Met Arg Leu Ile Se - #r Leu Ser Cys Asp Pro          210              - #   215              - #   220                          - - Asn Trp Gln Phe Ser Ile Asp Gly His Glu Le - #u Thr Ile Ile Glu Val      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Asp Gly Gln Leu Thr Glu Pro His Thr Val As - #p Arg Leu Gln Ile        Phe                                                                                             245  - #               250  - #               255             - - Thr Gly Gln Arg Tyr Ser Phe Val Leu Asp Al - #a Asn Gln Pro Val Asp                  260      - #           265      - #           270                  - - Asn Tyr Trp Ile Arg Ala Gln Pro Asn Lys Gl - #y Arg Asn Gly Leu Ala              275          - #       280          - #       285                      - - Gly Thr Phe Ala Asn Gly Val Asn Ser Ala Il - #e Leu Arg Tyr Ala Gly          290              - #   295              - #   300                          - - Ala Ala Asn Ala Asp Pro Thr Thr Ser Ala As - #n Pro Asn Pro Ala Gln      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Leu Asn Glu Ala Asp Leu His Ala Leu Ile As - #p Pro Ala Ala Pro        Gly                                                                                             325  - #               330  - #               335             - - Ile Pro Thr Pro Gly Ala Ala Asp Val Asn Le - #u Arg Phe Gln Leu Gly                  340      - #           345      - #           350                  - - Phe Ser Gly Gly Arg Phe Thr Ile Asn Gly Th - #r Ala Tyr Glu Ser Pro              355          - #       360          - #       365                      - - Ser Val Pro Thr Leu Leu Gln Ile Met Ser Gl - #y Ala Gln Ser Ala Asn          370              - #   375              - #   380                          - - Asp Leu Leu Pro Ala Gly Ser Val Tyr Glu Le - #u Pro Arg Asn Gln Val      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Val Glu Leu Val Val Pro Ala Gly Val Leu Gl - #y Gly Pro His Pro        Phe                                                                                             405  - #               410  - #               415             - - His Leu His Gly His Ala Phe Ser Val Val Ar - #g Ser Ala Gly Ser Ser                  420      - #           425      - #           430                  - - Thr Tyr Asn Phe Val Asn Pro Val Lys Arg As - #p Val Val Ser Leu Gly              435          - #       440          - #       445                      - - Val Thr Gly Asp Glu Val Thr Ile Arg Phe Va - #l Thr Asp Asn Pro Gly          450              - #   455              - #   460                          - - Pro Trp Phe Phe His Cys His Ile Glu Phe Hi - #s Leu Met Asn Gly Leu      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Ala Ile Val Phe Ala Glu Asp Met Ala Asn Th - #r Val Asp Ala Asn        Asn                                                                                             485  - #               490  - #               495             - - Pro Pro Val Glu Trp Ala Gln Leu Cys Glu Il - #e Tyr Asp Asp Leu Pro                  500      - #           505      - #           510                  - - Pro Glu Ala Thr Ser Ile Gln Thr Val Val Ar - #g Arg Ala Glu Pro Thr              515          - #       520          - #       525                      - - Gly Phe Ser Ala Lys Phe Arg Arg Glu Gly Le - #u                              530              - #   535                                                 - -  - - (2) INFORMATION FOR SEQ ID NO: 2:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 499 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #2:                           - - Gly Ile Gly Pro Val Ala Asp Leu Thr Ile Th - #r Asn Ala Ala Val Ser      1               5   - #                10  - #                15               - - Pro Asp Gly Phe Ser Arg Gln Ala Val Val Va - #l Asn Gly Gly Thr Pro                  20      - #            25      - #            30                   - - Gly Pro Leu Ile Thr Gly Asn Met Gly Asp Ar - #g Phe Gln Leu Asn Val              35          - #        40          - #        45                       - - Ile Asp Asn Leu Thr Asn His Thr Met Leu Ly - #s Ser Thr Ser Ile His          50              - #    55              - #    60                           - - Trp His Gly Phe Phe Gln Lys Gly Thr Asn Tr - #p Ala Asp Gly Pro Ala      65                  - #70                  - #75                  - #80        - - Phe Ile Asn Gln Cys Pro Ile Ser Ser Gly Hi - #s Ser Phe Leu Tyr Asp                      85  - #                90  - #                95               - - Phe Gln Val Pro Asp Gln Ala Gly Thr Phe Tr - #p Tyr His Ser His Leu                  100      - #           105      - #           110                  - - Ser Thr Gln Tyr Cys Asp Gly Leu Arg Gly Pr - #o Phe Val Val Tyr Asp              115          - #       120          - #       125                      - - Pro Asn Asp Pro Ala Ala Asp Leu Tyr Asp Va - #l Asp Asn Asp Asp Thr          130              - #   135              - #   140                          - - Val Ile Thr Leu Val Asp Trp Tyr His Val Al - #a Ala Lys Leu Gly Pro      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Ala Phe Pro Leu Gly Ala Asp Ala Thr Leu Il - #e Asn Gly Lys Gly        Arg                                                                                             165  - #               170  - #               175             - - Ser Pro Ser Thr Thr Thr Ala Asp Leu Ser Va - #l Ile Ser Val Thr Pro                  180      - #           185      - #           190                  - - Gly Lys Arg Tyr Arg Phe Arg Leu Val Ser Le - #u Ser Cys Asp Pro Asn              195          - #       200          - #       205                      - - Tyr Thr Phe Ser Ile Asp Gly His Asn Met Th - #r Ile Ile Glu Thr Asp          210              - #   215              - #   220                          - - Ser Ile Asn Thr Ala Pro Leu Val Val Asp Se - #r Ile Gln Ile Phe Ala      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Ala Gln Arg Tyr Ser Phe Val Leu Glu Ala As - #n Gln Ala Val Asp        Asn                                                                                             245  - #               250  - #               255             - - Tyr Trp Ile Arg Ala Asn Pro Asn Phe Gly As - #n Val Gly Phe Thr Gly                  260      - #           265      - #           270                  - - Gly Ile Asn Ser Ala Ile Leu Arg Tyr Asp Gl - #y Ala Ala Ala Val Glu              275          - #       280          - #       285                      - - Pro Thr Thr Thr Gln Thr Thr Ser Thr Ala Pr - #o Leu Asn Glu Val Asn          290              - #   295              - #   300                          - - Leu His Pro Leu Val Thr Thr Ala Val Pro Gl - #y Ser Pro Val Ala Gly      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Gly Val Asp Leu Ala Ile Asn Met Ala Phe As - #n Phe Asn Gly Thr        Asn                                                                                             325  - #               330  - #               335             - - Phe Phe Ile Asn Gly Ala Ser Phe Thr Pro Pr - #o Thr Val Pro Val Leu                  340      - #           345      - #           350                  - - Leu Gln Ile Ile Ser Gly Ala Gln Asn Ala Gl - #n Asp Leu Leu Pro Ser              355          - #       360          - #       365                      - - Gly Ser Val Tyr Ser Leu Pro Ser Asn Ala As - #p Ile Glu Ile Ser Phe          370              - #   375              - #   380                          - - Pro Ala Thr Ala Ala Ala Pro Gly Ala Pro Hi - #s Pro Phe His Leu His      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Gly His Ala Phe Ala Val Val Arg Ser Ala Gl - #y Ser Thr Val Tyr        Asn                                                                                             405  - #               410  - #               415             - - Tyr Asp Asn Pro Ile Phe Arg Asp Val Val Se - #r Thr Gly Thr Pro Ala                  420      - #           425      - #           430                  - - Ala Gly Asp Asn Val Thr Ile Arg Phe Arg Th - #r Asp Asn Pro Gly Pro              435          - #       440          - #       445                      - - Trp Phe Leu His Cys His Ile Asp Phe His Le - #u Glu Ala Gly Phe Ala          450              - #   455              - #   460                          - - Val Val Phe Ala Glu Asp Ile Pro Asp Val Al - #a Ser Ala Asn Pro Val      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Pro Gln Ala Trp Ser Asp Leu Cys Pro Thr Ty - #r Asp Ala Leu Asp        Pro                                                                                             485  - #               490  - #               495             - - Ser Asp Gln                                                               - -  - - (2) INFORMATION FOR SEQ ID NO: 3:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 499 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #3:                           - - Ala Ile Gly Pro Val Ala Ser Leu Val Val Al - #a Asn Ala Pro Val Ser      1               5   - #                10  - #                15               - - Pro Asp Gly Phe Leu Arg Asp Ala Ile Val Va - #l Asn Gly Val Val Pro                  20      - #            25      - #            30                   - - Ser Pro Leu Ile Thr Gly Lys Lys Gly Asp Ar - #g Phe Gln Leu Asn Val              35          - #        40          - #        45                       - - Val Asp Thr Leu Thr Asn His Ser Met Leu Ly - #s Ser Thr Ser Ile His          50              - #    55              - #    60                           - - Trp His Gly Phe Phe Gln Ala Gly Thr Asn Tr - #p Ala Glu Gly Pro Ala      65                  - #70                  - #75                  - #80        - - Phe Val Asn Gln Cys Pro Ile Ala Ser Gly Hi - #s Ser Phe Leu Tyr Asp                      85  - #                90  - #                95               - - Phe His Val Pro Asp Gln Ala Gly Thr Phe Tr - #p Tyr His Ser His Leu                  100      - #           105      - #           110                  - - Ser Thr Gln Tyr Cys Asp Gly Leu Arg Gly Pr - #o Phe Val Val Tyr Asp              115          - #       120          - #       125                      - - Pro Lys Asp Pro His Ala Ser Arg Tyr Asp Va - #l Asp Asn Glu Ser Thr          130              - #   135              - #   140                          - - Val Ile Thr Leu Thr Asp Trp Tyr His Thr Al - #a Ala Arg Leu Gly Pro      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Lys Phe Pro Leu Gly Ala Asp Ala Thr Leu Il - #e Asn Gly Leu Gly        Arg                                                                                             165  - #               170  - #               175             - - Ser Ala Ser Thr Pro Thr Ala Ala Leu Ala Va - #l Ile Asn Val Gln His                  180      - #           185      - #           190                  - - Gly Lys Arg Tyr Arg Phe Arg Leu Val Ser Il - #e Ser Cys Asp Pro Asn              195          - #       200          - #       205                      - - Tyr Thr Phe Ser Ile Asp Gly His Asn Leu Th - #r Val Ile Glu Val Asp          210              - #   215              - #   220                          - - Gly Ile Asn Ser Gln Pro Leu Leu Val Asp Se - #r Ile Gln Ile Phe Ala      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Ala Gln Arg Tyr Ser Phe Val Leu Asn Ala As - #n Gln Thr Val Gly        Asn                                                                                             245  - #               250  - #               255             - - Tyr Trp Val Arg Ala Asn Pro Asn Phe Gly Th - #r Val Gly Phe Ala Gly                  260      - #           265      - #           270                  - - Gly Ile Asn Ser Ala Ile Leu Arg Tyr Gln Gl - #y Ala Pro Val Ala Glu              275          - #       280          - #       285                      - - Pro Thr Thr Thr Gln Thr Pro Ser Val Ile Pr - #o Leu Ile Glu Thr Asn          290              - #   295              - #   300                          - - Leu His Pro Leu Ala Arg Met Pro Val Pro Gl - #y Ser Pro Thr Pro Gly      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Gly Val Asp Lys Ala Leu Asn Leu Ala Phe As - #n Phe Asn Gly Thr        Asn                                                                                             325  - #               330  - #               335             - - Phe Phe Ile Asn Asn Ala Thr Phe Thr Pro Pr - #o Thr Val Pro Val Leu                  340      - #           345      - #           350                  - - Leu Gln Ile Leu Ser Gly Ala Gln Thr Ala Gl - #n Asp Leu Leu Pro Ala              355          - #       360          - #       365                      - - Gly Ser Val Tyr Pro Leu Pro Ala His Ser Th - #r Ile Glu Ile Thr Leu          370              - #   375              - #   380                          - - Pro Ala Thr Ala Leu Ala Pro Gly Ala Pro Hi - #s Pro Phe His Leu His      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Gly His Ala Phe Ala Val Val Arg Ser Ala Gl - #y Ser Thr Thr Tyr        Asn                                                                                             405  - #               410  - #               415             - - Tyr Asn Asp Pro Ile Phe Arg Asp Val Val Se - #r Thr Gly Thr Pro Ala                  420      - #           425      - #           430                  - - Ala Gly Asp Asn Val Thr Ile Arg Phe Gln Th - #r Asp Asn Pro Gly Pro              435          - #       440          - #       445                      - - Trp Phe Leu His Cys His Ile Asp Phe His Le - #u Asp Ala Gly Phe Ala          450              - #   455              - #   460                          - - Ile Val Phe Ala Glu Asp Val Ala Asp Val Ly - #s Ala Ala Asn Pro Val      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Pro Lys Ala Trp Ser Asp Leu Cys Pro Ile Ty - #r Asp Gly Leu Ser        Glu                                                                                             485  - #               490  - #               495             - - Ala Asn Gln                                                               - -  - - (2) INFORMATION FOR SEQ ID NO: 4:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 548 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #4:                           - - Met His Thr Phe Leu Arg Ser Thr Ala Leu Va - #l Val Ala Gly Leu Ser      1               5   - #                10  - #                15               - - Ala Arg Ala Leu Ala Ser Ile Gly Pro Val Th - #r Asp Phe His Ile Val                  20      - #            25      - #            30                   - - Asn Ala Ala Val Ser Pro Asp Gly Phe Ser Ar - #g Gln Ala Val Leu Ala              35          - #        40          - #        45                       - - Glu Gly Val Phe Pro Gly Pro Leu Ile Ala Gl - #y Asn Lys Gly Asp Asn          50              - #    55              - #    60                           - - Phe Gln Ile Asn Val Ile Asp Glu Leu Thr As - #n Ala Thr Met Leu Lys      65                  - #70                  - #75                  - #80        - - Thr Thr Thr Ile His Trp His Gly Phe Phe Gl - #n His Gly Thr Asn Trp                      85  - #                90  - #                95               - - Ala Asp Gly Pro Ala Phe Ile Asn Gln Cys Pr - #o Ile Ala Ser Gly Asp                  100      - #           105      - #           110                  - - Ser Phe Leu Tyr Asn Phe Gln Val Pro Asp Gl - #n Ala Gly Thr Phe Trp              115          - #       120          - #       125                      - - Tyr His Ser His Leu Ser Thr Gln Tyr Cys As - #p Gly Leu Arg Gly Pro          130              - #   135              - #   140                          - - Phe Val Val Tyr Asp Pro Ala Asp Pro Tyr Le - #u Asp Gln Tyr Asp Val      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Asp Asp Asp Ser Thr Val Ile Thr Leu Ala As - #p Trp Tyr His Thr        Ala                                                                                             165  - #               170  - #               175             - - Ala Arg Leu Gly Ser Pro Phe Pro Ala Ala As - #p Thr Thr Leu Ile Asn                  180      - #           185      - #           190                  - - Gly Leu Gly Arg Cys Gly Glu Ala Gly Cys Pr - #o Val Ser Asp Leu Ala              195          - #       200          - #       205                      - - Val Ile Ser Val Thr Lys Gly Lys Arg Tyr Ar - #g Phe Arg Leu Val Ser          210              - #   215              - #   220                          - - Ile Ser Cys Asp Ser Phe Phe Thr Phe Ser Il - #e Asp Gly His Ser Leu      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Asn Val Ile Glu Val Asp Ala Thr Asn His Gl - #n Pro Leu Thr Val        Asp                                                                                             245  - #               250  - #               255             - - Glu Leu Thr Ile Tyr Ala Gly Gln Arg Tyr Se - #r Phe Ile Leu Thr Ala                  260      - #           265      - #           270                  - - Asp Gln Asp Val Asp Asn Tyr Trp Ile Arg Al - #a Asn Pro Gly Ile Gly              275          - #       280          - #       285                      - - Ile Thr Thr Gly Phe Ala Gly Gly Ile Asn Se - #r Ala Ile Leu Arg Tyr          290              - #   295              - #   300                          - - Asp Gly Ala Asp Val Val Glu Pro Thr Thr Th - #r Gln Ala Thr Ser Pro      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Val Val Leu Ser Glu Ser Asn Leu Ala Pro Le - #u Thr Asn Ala Ala        Ala                                                                                             325  - #               330  - #               335             - - Pro Gly Leu Pro Glu Val Gly Gly Val Asp Le - #u Ala Leu Asn Phe Asn                  340      - #           345      - #           350                  - - Leu Thr Phe Asp Gly Pro Ser Leu Lys Phe Gl - #n Ile Asn Gly Val Thr              355          - #       360          - #       365                      - - Phe Val Pro Pro Thr Val Pro Val Leu Leu Gl - #n Ile Leu Ser Gly Ala          370              - #   375              - #   380                          - - Gln Ser Ala Ala Asp Leu Leu Pro Ser Gly Se - #r Val Tyr Ala Leu Pro      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Ser Asn Ala Thr Ile Glu Leu Ser Leu Pro Al - #a Gly Ala Leu Gly        Gly                                                                                             405  - #               410  - #               415             - - Pro His Pro Phe His Leu His Gly His Thr Ph - #e Ser Val Val Arg Pro                  420      - #           425      - #           430                  - - Ala Gly Ser Thr Thr Tyr Asn Tyr Val Asn Pr - #o Val Gln Arg Asp Val              435          - #       440          - #       445                      - - Val Ser Ile Gly Asn Thr Gly Asp Asn Val Th - #r Ile Arg Phe Asp Thr          450              - #   455              - #   460                          - - Asn Asn Pro Gly Pro Trp Phe Leu His Cys Hi - #s Ile Asp Trp His Leu      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Glu Ala Ala Leu Pro Leu Ser Ser Leu Arg Th - #r Ser Leu Thr Leu        Arg                                                                                             485  - #               490  - #               495             - - Pro Leu Thr Leu Ser Pro Arg Thr Gly Pro Th - #r Cys Ala Leu Ser Thr                  500      - #           505      - #           510                  - - Thr Leu Trp Thr His Leu Ile Thr Ser Gly Ph - #e Ala Ser Ile Ile Gln              515          - #       520          - #       525                      - - Trp Met Met Gly Gly Asn Gly Leu Phe Ala Pr - #o His Ala Leu Ser Phe          530              - #   535              - #   540                          - - Leu Gly Ser Gln                                                          545                                                                            - -  - - (2) INFORMATION FOR SEQ ID NO: 5:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 529 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #5:                           - - Met Leu Ser Ser Ile Thr Leu Leu Pro Leu Le - #u Ala Ala Val Ser Thr      1               5   - #                10  - #                15               - - Pro Ala Phe Ala Ala Val Arg Asn Tyr Lys Ph - #e Asp Ile Lys Asn Val                  20      - #            25      - #            30                   - - Asn Val Ala Pro Asp Gly Phe Gln Arg Ser Il - #e Val Ser Val Asn Gly              35          - #        40          - #        45                       - - Leu Val Pro Gly Thr Leu Ile Thr Ala Asn Ly - #s Gly Asp Thr Leu Arg          50              - #    55              - #    60                           - - Ile Asn Val Thr Asn Gln Leu Thr Asp Pro Se - #r Met Arg Arg Ala Thr      65                  - #70                  - #75                  - #80        - - Thr Ile His Trp His Gly Leu Phe Gln Ala Th - #r Thr Ala Asp Glu Asp                      85  - #                90  - #                95               - - Gly Pro Ala Phe Val Thr Gln Cys Pro Ile Al - #a Gln Asn Leu Ser Tyr                  100      - #           105      - #           110                  - - Thr Tyr Glu Ile Pro Leu Arg Gly Gln Thr Gl - #y Thr Met Trp Tyr His              115          - #       120          - #       125                      - - Ala His Leu Ala Ser Gln Tyr Val Asp Gly Le - #u Arg Gly Pro Leu Val          130              - #   135              - #   140                          - - Ile Tyr Asp Pro Asn Asp Pro His Lys Ser Ar - #g Tyr Asp Val Asp Asp      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Ala Ser Thr Val Val Met Leu Glu Asp Trp Ty - #r His Thr Pro Ala        Pro                                                                                             165  - #               170  - #               175             - - Val Leu Glu Lys Gln Met Phe Ser Thr Asn As - #n Thr Ala Leu Leu Ser                  180      - #           185      - #           190                  - - Pro Val Pro Asp Ser Gly Leu Ile Asn Gly Ly - #s Gly Arg Tyr Val Gly              195          - #       200          - #       205                      - - Gly Pro Ala Val Pro Arg Ser Val Ile Asn Va - #l Lys Arg Gly Lys Arg          210              - #   215              - #   220                          - - Tyr Arg Leu Arg Val Ile Asn Ala Ser Ala Il - #e Gly Ser Phe Thr Phe      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Ser Ile Glu Gly His Ser Leu Thr Val Ile Gl - #u Ala Asp Gly Ile        Leu                                                                                             245  - #               250  - #               255             - - His Gln Pro Leu Ala Val Asp Ser Phe Gln Il - #e Tyr Ala Gly Gln Arg                  260      - #           265      - #           270                  - - Tyr Ser Val Ile Val Glu Ala Asn Gln Thr Al - #a Ala Asn Tyr Trp Ile              275          - #       280          - #       285                      - - Arg Ala Pro Met Thr Val Ala Gly Ala Gly Th - #r Asn Ala Asn Leu Asp          290              - #   295              - #   300                          - - Pro Thr Asn Val Phe Ala Val Leu His Tyr Gl - #u Gly Ala Pro Asn Ala      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Glu Pro Thr Thr Glu Gln Gly Ser Ala Ile Gl - #y Thr Ala Leu Val        Glu                                                                                             325  - #               330  - #               335             - - Glu Asn Leu His Ala Leu Ile Asn Pro Gly Al - #a Pro Gly Gly Ser Ala                  340      - #           345      - #           350                  - - Pro Ala Asp Val Ser Leu Asn Leu Ala Ile Gl - #y Arg Ser Thr Val Asp              355          - #       360          - #       365                      - - Gly Ile Leu Arg Phe Thr Phe Asn Asn Ile Ly - #s Tyr Glu Ala Pro Ser          370              - #   375              - #   380                          - - Leu Pro Thr Leu Leu Lys Ile Leu Ala Asn As - #n Ala Ser Asn Asp Ala      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Asp Phe Thr Pro Asn Glu His Thr Ile Val Le - #u Pro His Asn Lys        Val                                                                                             405  - #               410  - #               415             - - Ile Glu Leu Asn Ile Thr Gly Gly Ala Asp Hi - #s Pro Ile His Leu His                  420      - #           425      - #           430                  - - Gly His Val Phe Asp Ile Val Lys Ser Leu Gl - #y Gly Thr Pro Asn Tyr              435          - #       440          - #       445                      - - Val Asn Pro Pro Arg Arg Asp Val Val Arg Va - #l Gly Gly Thr Gly Val          450              - #   455              - #   460                          - - Val Leu Arg Phe Lys Thr Asp Asn Pro Gly Pr - #o Trp Phe Val His Cys      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - His Ile Asp Trp His Leu Glu Ala Gly Leu Al - #a Leu Val Phe Ala        Glu                                                                                             485  - #               490  - #               495             - - Ala Pro Ser Gln Ile Arg Gln Gly Val Gln Se - #r Val Gln Pro Asn Asn                  500      - #           505      - #           510                  - - Ala Trp Asn Gln Leu Cys Pro Lys Tyr Ala Al - #a Leu Pro Pro Asp Leu              515          - #       520          - #       525                      - - Gln                                                                       - -  - - (2) INFORMATION FOR SEQ ID NO: 6:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 599 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #6:                           - - Met Ala Arg Ser Thr Thr Ser Leu Phe Ala Le - #u Ser Leu Val Ala Ser      1               5   - #                10  - #                15               - - Ala Phe Ala Arg Val Val Asp Tyr Gly Phe As - #p Val Ala Asn Gly Ala                  20      - #            25      - #            30                   - - Val Ala Pro Asp Gly Val Thr Arg Asn Ala Va - #l Leu Val Asn Gly Arg              35          - #        40          - #        45                       - - Phe Pro Gly Pro Leu Ile Thr Ala Asn Lys Gl - #y Asp Thr Leu Lys Ile          50              - #    55              - #    60                           - - Thr Val Arg Asn Lys Leu Ser Asp Pro Thr Me - #t Arg Arg Ser Thr Thr      65                  - #70                  - #75                  - #80        - - Ile His Trp His Gly Leu Leu Gln His Arg Th - #r Ala Glu Glu Asp Gly                      85  - #                90  - #                95               - - Pro Ala Phe Val Thr Gln Cys Pro Ile Pro Pr - #o Gln Glu Ser Tyr Thr                  100      - #           105      - #           110                  - - Tyr Thr Met Pro Leu Gly Glu Gln Thr Gly Th - #r Tyr Trp Tyr His Ser              115          - #       120          - #       125                      - - His Leu Ser Ser Gln Tyr Val Asp Gly Leu Ar - #g Gly Pro Ile Val Ile          130              - #   135              - #   140                          - - Tyr Asp Pro His Asp Pro Tyr Arg Asn Tyr Ty - #r Asp Val Asp Asp Glu      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Arg Thr Val Phe Thr Leu Ala Asp Trp Tyr Hi - #s Thr Pro Ser Glu        Ala                                                                                             165  - #               170  - #               175             - - Ile Ile Ala Thr His Asp Val Leu Lys Thr Il - #e Pro Asp Ser Gly Thr                  180      - #           185      - #           190                  - - Ile Asn Gly Lys Gly Lys Tyr Asp Pro Ala Se - #r Ala Asn Thr Asn Asn              195          - #       200          - #       205                      - - Thr Thr Leu Glu Asn Leu Tyr Thr Leu Lys Va - #l Lys Arg Gly Lys Arg          210              - #   215              - #   220                          - - Tyr Arg Leu Arg Ile Ile Asn Ala Ser Ala Il - #e Ala Ser Phe Arg Phe      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Gly Val Gln Gly His Lys Cys Thr Ile Ile Gl - #u Ala Asp Gly Val        Leu                                                                                             245  - #               250  - #               255             - - Thr Lys Pro Ile Glu Val Asp Ala Phe Asp Il - #e Leu Ala Gly Gln Arg                  260      - #           265      - #           270                  - - Tyr Ser Cys Ile Leu Lys Ala Asp Gln Asp Pr - #o Asp Ser Tyr Trp Ile              275          - #       280          - #       285                      - - Asn Ala Pro Ile Thr Asn Val Leu Asn Thr As - #n Val Gln Ala Leu Leu          290              - #   295              - #   300                          - - Val Tyr Glu Asp Asp Lys Arg Pro Thr His Ty - #r Pro Trp Lys Pro Phe      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Leu Thr Trp Lys Ile Ser Asn Glu Ile Ile Gl - #n Tyr Trp Gln His        Lys                                                                                             325  - #               330  - #               335             - - His Gly Ser His Gly His Lys Gly Lys Gly Hi - #s His His Lys Val Arg                  340      - #           345      - #           350                  - - Ala Ile Gly Gly Val Ser Gly Leu Ser Ser Ar - #g Val Lys Ser Arg Ala              355          - #       360          - #       365                      - - Ser Asp Leu Ser Lys Lys Ala Val Glu Leu Al - #a Ala Ala Leu Val Ala          370              - #   375              - #   380                          - - Gly Glu Ala Glu Leu Asp Lys Arg Gln Asn Gl - #u Asp Asn Ser Thr Ile      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Val Leu Asp Glu Thr Lys Leu Ile Pro Leu Va - #l Gln Pro Gly Ala        Pro                                                                                             405  - #               410  - #               415             - - Gly Gly Ser Arg Pro Ala Asp Val Val Val Pr - #o Leu Asp Phe Gly Leu                  420      - #           425      - #           430                  - - Asn Phe Ala Asn Gly Leu Trp Thr Ile Asn As - #n Val Ser Tyr Ser Pro              435          - #       440          - #       445                      - - Pro Asp Val Pro Thr Leu Leu Lys Ile Leu Th - #r Asp Lys Asp Lys Val          450              - #   455              - #   460                          - - Asp Ala Ser Asp Phe Thr Ala Asp Glu His Th - #r Tyr Ile Leu Pro Lys      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Asn Gln Val Val Glu Leu His Ile Lys Gly Gl - #n Ala Leu Gly Ile        Val                                                                                             485  - #               490  - #               495             - - His Pro Leu His Leu His Gly His Ala Phe As - #p Val Val Gln Phe Gly                  500      - #           505      - #           510                  - - Asp Asn Ala Pro Asn Tyr Val Asn Pro Pro Ar - #g Arg Asp Val Val Gly              515          - #       520          - #       525                      - - Val Thr Asp Ala Gly Val Arg Ile Gln Phe Ar - #g Thr Asp Asn Pro Gly          530              - #   535              - #   540                          - - Pro Trp Phe Leu His Cys His Ile Asp Trp Hi - #s Leu Glu Glu Gly Phe      545                 5 - #50                 5 - #55                 5 -      #60                                                                              - - Ala Met Val Phe Ala Glu Ala Pro Glu Asp Il - #e Lys Lys Gly Ser        Gln                                                                                             565  - #               570  - #               575             - - Ser Val Lys Pro Asp Gly Gln Trp Lys Lys Le - #u Cys Glu Lys Tyr Glu                  580      - #           585      - #           590                  - - Lys Leu Pro Glu Ala Leu Gln                                                      595                                                                    - -  - - (2) INFORMATION FOR SEQ ID NO: 7:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 572 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #7:                           - - Met Ala Arg Thr Thr Phe Leu Val Ser Val Se - #r Leu Phe Val Ser Ala      1               5   - #                10  - #                15               - - Val Leu Ala Arg Thr Val Glu Tyr Asn Leu Ly - #s Ile Ser Asn Gly Lys                  20      - #            25      - #            30                   - - Ile Ala Pro Asp Gly Val Glu Arg Asp Ala Th - #r Leu Val Asn Gly Gly              35          - #        40          - #        45                       - - Tyr Pro Gly Pro Leu Ile Phe Ala Asn Lys Gl - #y Asp Thr Leu Lys Val          50              - #    55              - #    60                           - - Lys Val Gln Asn Lys Leu Thr Asn Pro Asp Me - #t Tyr Arg Thr Thr Ser      65                  - #70                  - #75                  - #80        - - Ile His Trp His Gly Leu Leu Gln His Arg As - #n Ala Asp Asp Asp Gly                      85  - #                90  - #                95               - - Pro Ala Phe Val Thr Gln Cys Pro Ile Val Pr - #o Gln Ala Ser Tyr Thr                  100      - #           105      - #           110                  - - Tyr Thr Met Pro Leu Gly Asp Gln Thr Gly Th - #r Tyr Trp Tyr His Ser              115          - #       120          - #       125                      - - His Leu Ser Ser Gln Tyr Val Asp Gly Leu Ar - #g Gly Pro Leu Val Ile          130              - #   135              - #   140                          - - Tyr Asp Pro Lys Asp Pro His Arg Arg Leu Ty - #r Asp Ile Asp Asp Glu      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Lys Thr Val Leu Ile Ile Gly Asp Trp Tyr Hi - #s Thr Ser Ser Lys        Ala                                                                                             165  - #               170  - #               175             - - Ile Leu Ala Thr Gly Asn Ile Thr Leu Gln Gl - #n Pro Asp Ser Ala Thr                  180      - #           185      - #           190                  - - Ile Asn Gly Lys Gly Arg Phe Asp Pro Asp As - #n Thr Pro Ala Asn Pro              195          - #       200          - #       205                      - - Asn Thr Leu Tyr Thr Leu Lys Val Lys Arg Gl - #y Lys Arg Tyr Arg Leu          210              - #   215              - #   220                          - - Arg Val Ile Asn Ser Ser Ala Ile Ala Ser Ph - #e Arg Met Ser Ile Gln      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Gly His Lys Met Thr Val Ile Ala Ala Asp Gl - #y Val Ser Thr Lys        Pro                                                                                             245  - #               250  - #               255             - - Tyr Gln Val Asp Ser Phe Asp Ile Leu Ala Gl - #y Gln Arg Ile Asp Ala                  260      - #           265      - #           270                  - - Val Val Glu Ala Asn Gln Glu Pro Asp Thr Ty - #r Trp Ile Asn Ala Pro              275          - #       280          - #       285                      - - Leu Thr Asn Val Ala Asn Lys Thr Ala Gln Al - #a Leu Leu Ile Tyr Glu          290              - #   295              - #   300                          - - Asp Asp Arg Arg Pro Tyr His Pro Pro Lys Gl - #y Pro Tyr Arg Lys Trp      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Ser Val Ser Glu Ala Ile Ile Lys Tyr Trp Ly - #s His Lys His Gly        Arg                                                                                             325  - #               330  - #               335             - - Gly Leu Leu Ser Gly His Gly Gly Leu Lys Al - #a Arg Met Met Glu Gly                  340      - #           345      - #           350                  - - Ser Leu His Leu His Gly Arg Arg Asp Ile Va - #l Lys Arg Gln Asn Glu              355          - #       360          - #       365                      - - Thr Thr Thr Val Val Met Asp Glu Thr Lys Le - #u Val Pro Leu Glu His          370              - #   375              - #   380                          - - Pro Gly Ala Ala Cys Gly Ser Lys Pro Ala As - #p Leu Val Ile Asp Leu      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Thr Phe Gly Val Asn Phe Thr Thr Gly His Tr - #p Met Ile Asn Gly        Ile                                                                                             405  - #               410  - #               415             - - Pro His Lys Ser Pro Asp Met Pro Thr Leu Le - #u Lys Ile Leu Thr Asp                  420      - #           425      - #           430                  - - Thr Asp Gly Val Thr Glu Ser Asp Phe Thr Gl - #n Pro Glu His Thr Ile              435          - #       440          - #       445                      - - Ile Leu Pro Lys Asn Lys Cys Val Glu Phe As - #n Ile Lys Gly Asn Ser          450              - #   455              - #   460                          - - Gly Leu Gly Ile Val His Pro Ile His Leu Hi - #s Gly His Thr Phe Asp      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Val Val Gln Phe Gly Asn Asn Pro Pro Asn Ty - #r Val Asn Pro Pro        Arg                                                                                             485  - #               490  - #               495             - - Arg Asp Val Val Gly Ala Thr Asp Glu Gly Va - #l Arg Phe Gln Phe Lys                  500      - #           505      - #           510                  - - Thr Asp Asn Pro Gly Pro Trp Phe Leu His Cy - #s His Ile Asp Trp His              515          - #       520          - #       525                      - - Leu Glu Glu Gly Phe Ala Met Val Phe Ala Gl - #u Ala Pro Glu Ala Ile          530              - #   535              - #   540                          - - Lys Gly Gly Pro Lys Ser Val Pro Val Asp Ar - #g Gln Trp Lys Asp Leu      545                 5 - #50                 5 - #55                 5 -      #60                                                                              - - Cys Arg Lys Tyr Gly Ser Leu Pro Ala Gly Ph - #e Leu                                      565  - #               570                                     - -  - - (2) INFORMATION FOR SEQ ID NO: 8:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 575 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #8:                           - - Met Ala Arg Thr Thr Phe Leu Val Ser Val Se - #r Leu Phe Val Ser        Ala                                                                             1               5   - #                10  - #                15              - - Val Leu Ala Arg Thr Val Glu Tyr Gly Leu Ly - #s Ile Ser Asp Gly Glu                  20      - #            25      - #            30                   - - Ile Ala Pro Asp Gly Val Lys Arg Asn Ala Th - #r Leu Val Asn Gly Gly              35          - #        40          - #        45                       - - Tyr Pro Gly Pro Leu Ile Phe Ala Asn Lys Gl - #y Asp Thr Leu Lys Val          50              - #    55              - #    60                           - - Lys Val Gln Asn Lys Leu Thr Asn Pro Glu Me - #t Tyr Arg Thr Thr Ser      65                  - #70                  - #75                  - #80        - - Ile His Trp His Gly Leu Leu Gln His Arg As - #n Ala Asp Asp Asp Gly                      85  - #                90  - #                95               - - Pro Ser Phe Val Thr Gln Cys Pro Ile Val Pr - #o Arg Glu Ser Tyr Thr                  100      - #           105      - #           110                  - - Tyr Thr Ile Pro Leu Asp Asp Gln Thr Gly Th - #r Tyr Trp Tyr His Ser              115          - #       120          - #       125                      - - His Leu Ser Ser Gln Tyr Val Asp Gly Leu Ar - #g Gly Pro Leu Val Ile          130              - #   135              - #   140                          - - Tyr Pro Lys Asp Pro His Arg Arg Leu Tyr As - #p Val Asp Asp Glu Lys      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Thr Val Leu Ile Ile Gly Asp Trp Tyr His Gl - #u Ser Ser Lys Ala        Ile                                                                                             165  - #               170  - #               175             - - Leu Ala Ser Gly Asn Ile Thr Arg Gln Arg Pr - #o Val Ser Ala Thr Ile                  180      - #           185      - #           190                  - - Asn Gly Lys Gly Arg Phe Asp Pro Asp Asn Th - #r Pro Ala Asn Pro Asp              195          - #       200          - #       205                      - - Thr Leu Tyr Thr Leu Lys Val Lys Arg Gly Ly - #s Arg Tyr Arg Leu Arg          210              - #   215              - #   220                          - - Val Ile Asn Ser Ser Glu Ile Ala Ser Phe Ar - #g Phe Ser Val Glu Gly      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - His Lys Val Thr Val Ile Ala Ala Asp Gly Va - #l Ser Thr Lys Pro        Tyr                                                                                             245  - #               250  - #               255             - - Gln Val Asp Ala Phe Asp Ile Leu Ala Gly Gl - #n Arg Ile Asp Cys Val                  260      - #           265      - #           270                  - - Val Glu Ala Asn Gln Glu Pro Asp Thr Tyr Tr - #p Ile Asn Ala Pro Leu              275          - #       280          - #       285                      - - Thr Asn Val Pro Asn Lys Thr Ala Gln Ala Le - #u Leu Val Tyr Glu Glu          290              - #   295              - #   300                          - - Asp Arg Arg Pro Tyr His Pro Pro Lys Gly Pr - #o Tyr Arg Lys Trp Ser      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Val Ser Glu Ala Ile Ile Lys Tyr Trp Asn Hi - #s Lys His Lys His        Gly                                                                                             325  - #               330  - #               335             - - Arg Gly Leu Leu Ser Gly His Gly Gly Leu Ly - #s Ala Arg Met Ile Glu                  340      - #           345      - #           350                  - - Gly Ser His His Leu His Ser Arg Ser Val Va - #l Lys Arg Gln Asn Glu              355          - #       360          - #       365                      - - Thr Thr Thr Val Val Met Asp Glu Ser Lys Le - #u Val Pro Leu Glu Tyr          370              - #   375              - #   380                          - - Pro Gly Ala Ala Cys Gly Ser Lys Pro Ala As - #p Leu Val Leu Asp Leu      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Thr Phe Gly Leu Asn Phe Ala Thr Gly His Tr - #p Met Ile Asn Gly        Ile                                                                                             405  - #               410  - #               415             - - Pro Tyr Glu Ser Pro Lys Ile Pro Thr Leu Le - #u Lys Ile Leu Thr Asp                  420      - #           425      - #           430                  - - Glu Asp Gly Val Thr Glu Ser Asp Phe Thr Ly - #s Glu Glu His Thr Val              435          - #       440          - #       445                      - - Ile Leu Pro Lys Asn Lys Cys Ile Glu Phe As - #n Ile Lys Gly Asn Ser          450              - #   455              - #   460                          - - Gly Ile Pro Ile Thr His Pro Val His Leu Hi - #s Gly His Thr Trp Asp      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Val Val Gln Phe Gly Asn Asn Pro Pro Asn Ty - #r Val Asn Pro Pro        Arg                                                                                             485  - #               490  - #               495             - - Arg Asp Val Val Gly Ser Thr Asp Ala Gly Va - #l Arg Ile Gln Phe Lys                  500      - #           505      - #           510                  - - Thr Asp Asn Pro Gly Pro Trp Phe Leu His Cy - #s His Ile Asp Trp His              515          - #       520          - #       525                      - - Leu Glu Glu Gly Phe Ala Met Val Phe Ala Gl - #u Ala Pro Glu Ala Val          530              - #   535              - #   540                          - - Lys Gly Gly Pro Lys Ser Val Ala Val Asp Se - #r Gln Trp Glu Gly Leu      545                 5 - #50                 5 - #55                 5 -      #60                                                                              - - Cys Gly Lys Tyr Asp Asn Trp Leu Lys Ser As - #n Pro Gly Gln Leu                         565  - #               570  - #               575              - -  - - (2) INFORMATION FOR SEQ ID NO: 9:                                    - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 616 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #9:                           - - Met Lys Arg Phe Phe Ile Asn Ser Leu Leu Le - #u Leu Ala Gly Leu Leu      1               5   - #                10  - #                15               - - Asn Ser Gly Ala Leu Ala Ala Pro Ser Thr Hi - #s Pro Arg Ser Asn Pro                  20      - #            25      - #            30                   - - Asp Ile Leu Leu Glu Arg Asp Asp His Ser Le - #u Thr Ser Arg Gln Gly              35          - #        40          - #        45                       - - Ser Cys His Ser Pro Ser Asn Arg Ala Cys Tr - #p Cys Ser Gly Phe Asp          50              - #    55              - #    60                           - - Ile Asn Thr Asp Tyr Glu Thr Lys Thr Pro As - #n Thr Gly Val Val Arg      65                  - #70                  - #75                  - #80        - - Arg Tyr Thr Phe Asp Ile Thr Glu Val Asp As - #n Arg Pro Gly Pro Asp                      85  - #                90  - #                95               - - Gly Val Ile Lys Glu Lys Leu Met Leu Ile As - #n Asp Lys Leu Leu Gly                  100      - #           105      - #           110                  - - Pro Thr Val Phe Ala Asn Trp Gly Asp Thr Il - #e Glu Val Thr Val Asn              115          - #       120          - #       125                      - - Asn His Leu Arg Thr Asn Gly Thr Ser Ile Hi - #s Trp His Gly Leu His          130              - #   135              - #   140                          - - Gln Lys Gly Thr Asn Tyr His Asp Gly Ala As - #n Gly Val Thr Glu Cys      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Pro Ile Pro Pro Gly Gly Ser Arg Val Tyr Se - #r Phe Arg Ala Arg        Gln                                                                                             165  - #               170  - #               175             - - Tyr Gly Thr Ser Trp Tyr His Ser His Phe Se - #r Ala Gln Tyr Gly Asn                  180      - #           185      - #           190                  - - Gly Val Ser Gly Ala Ile Gln Ile Asn Gly Pr - #o Ala Ser Leu Pro Tyr              195          - #       200          - #       205                      - - Asp Ile Asp Leu Gly Val Leu Pro Leu Xaa As - #p Trp Tyr Tyr Lys Ser          210              - #   215              - #   220                          - - Ala Asp Gln Leu Val Ile Glu Thr Leu Xaa Ly - #s Gly Asn Ala Pro Phe      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Ser Asp Asn Val Leu Ile Asn Gly Thr Ala Ly - #s His Pro Thr Thr        Gly                                                                                             245  - #               250  - #               255             - - Glu Gly Glu Tyr Ala Ile Val Lys Leu Thr Pr - #o Asp Lys Arg His Arg                  260      - #           265      - #           270                  - - Leu Arg Leu Ile Asn Met Ser Val Glu Asn Hi - #s Phe Gln Val Ser Leu              275          - #       280          - #       285                      - - Ala Lys His Thr Met Thr Val Ile Ala Ala As - #p Met Val Pro Val Asn          290              - #   295              - #   300                          - - Ala Met Thr Val Asp Ser Leu Phe Met Ala Va - #l Gly Gln Arg Tyr Asp      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Val Thr Ile Asp Ala Ser Gln Ala Val Gly As - #n Tyr Trp Phe Asn        Ile                                                                                             325  - #               330  - #               335             - - Thr Phe Gly Gly Gln Gln Lys Cys Gly Phe Se - #r His Asn Pro Ala Pro                  340      - #           345      - #           350                  - - Ala Ala Ile Phe Arg Tyr Glu Gly Ala Pro As - #p Ala Leu Pro Thr Asp              355          - #       360          - #       365                      - - Pro Gly Ala Ala Pro Lys Asp His Gln Cys Le - #u Asp Thr Leu Asp Leu          370              - #   375              - #   380                          - - Ser Pro Val Val Gln Lys Asn Val Pro Val As - #p Gly Phe Val Lys Glu      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Pro Gly Asn Thr Leu Pro Val Thr Leu His Va - #l Asp Gln Ala Ala        Ala                                                                                             405  - #               410  - #               415             - - Pro His Val Phe Thr Trp Lys Ile Asn Gly Se - #r Ala Ala Asp Val Asp                  420      - #           425      - #           430                  - - Trp Asp Arg Pro Val Leu Glu Tyr Val Met As - #n Asn Asp Leu Ser Ser              435          - #       440          - #       445                      - - Ile Pro Val Lys Asn Asn Ile Val Arg Val As - #p Gly Val Asn Glu Trp          450              - #   455              - #   460                          - - Thr Tyr Trp Leu Val Glu Asn Asp Pro Glu Gl - #y Arg Leu Ser Leu Pro      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - His Pro Met His Leu His Gly His Asp Phe Ph - #e Val Leu Gly Arg        Ser                                                                                             485  - #               490  - #               495             - - Pro Asp Val Ser Pro Asp Ser Glu Thr Arg Ph - #e Val Phe Asp Pro Ala                  500      - #           505      - #           510                  - - Val Asp Leu Pro Arg Leu Arg Gly His Asn Pr - #o Val Arg Arg Asp Val              515          - #       520          - #       525                      - - Thr Met Leu Pro Ala Arg Gly Trp Leu Leu Le - #u Ala Phe Arg Thr Asp          530              - #   535              - #   540                          - - Asn Pro Gly Ala Trp Leu Phe His Cys His Il - #e Ala Xaa His Val Ser      545                 5 - #50                 5 - #55                 5 -      #60                                                                              - - Gly Gly Leu Ser Val Asp Phe Leu Glu Arg Pr - #o Asp Glu Leu Arg        Gly                                                                                             565  - #               570  - #               575             - - Gln Leu Thr Gly Glu Ser Lys Ala Glu Leu Gl - #u Arg Val Cys Arg Glu                  580      - #           585      - #           590                  - - Trp Lys Asp Trp Glu Ala Lys Ser Pro His Gl - #y Lys Ile Asp Ser Gly              595          - #       600          - #       605                      - - Leu Lys Gln Arg Arg Trp Asp Ala                                              610              - #   615                                                 - -  - - (2) INFORMATION FOR SEQ ID NO: 10:                                   - -      (i) SEQUENCE CHARACTERISTICS:                                                 (A) LENGTH: 573 amino - #acids                                                (B) TYPE: amino acid                                                          (C) STRANDEDNESS: single                                                      (D) TOPOLOGY: linear                                                 - -     (ii) MOLECULE TYPE: protein                                           - -     (xi) SEQUENCE DESCRIPTION: SEQ ID NO: - #10:                          - - Gln Gln Ser Cys Asn Thr Pro Ser Asn Arg Al - #a Cys Trp Thr Asp Gly      1               5   - #                10  - #                15               - - Tyr Asp Ile Asn Thr Asp Tyr Glu Val Asp Se - #r Pro Asp Thr Gly Val                  20      - #            25      - #            30                   - - Val Arg Pro Tyr Thr Leu Thr Leu Thr Glu Va - #l Asp Asn Trp Thr Gly              35          - #        40          - #        45                       - - Pro Asp Gly Val Val Lys Glu Lys Val Met Le - #u Val Asn Asn Ser Ile          50              - #    55              - #    60                           - - Ile Gly Pro Thr Ile Phe Ala Asp Trp Gly As - #p Thr Ile Gln Val Thr      65                  - #70                  - #75                  - #80        - - Val Ile Asn Asn Leu Glu Thr Asn Gly Thr Se - #r Ile His Trp His Gly                      85  - #                90  - #                95               - - Leu His Gln Lys Gly Thr Asn Leu His Asp Gl - #y Ala Asn Gly Ile Thr                  100      - #           105      - #           110                  - - Glu Cys Pro Ile Pro Pro Lys Gly Gly Arg Ly - #s Val Tyr Arg Phe Lys              115          - #       120          - #       125                      - - Ala Gln Gln Tyr Gly Thr Ser Trp Tyr His Se - #r His Phe Ser Ala Gln          130              - #   135              - #   140                          - - Tyr Gly Asn Gly Val Val Gly Ala Ile Gln Il - #e Asn Gly Pro Ala Ser      145                 1 - #50                 1 - #55                 1 -      #60                                                                              - - Leu Pro Tyr Asp Thr Asp Leu Gly Val Phe Pr - #o Ile Ser Asp Tyr        Tyr                                                                                             165  - #               170  - #               175             - - Tyr Ser Ser Ala Asp Glu Leu Val Glu Leu Th - #r Lys Asn Ser Gly Ala                  180      - #           185      - #           190                  - - Pro Phe Ser Asp Asn Val Leu Phe Asn Gly Th - #r Ala Lys His Pro Glu              195          - #       200          - #       205                      - - Thr Gly Glu Gly Glu Tyr Ala Asn Val Thr Le - #u Thr Pro Gly Arg Arg          210              - #   215              - #   220                          - - His Arg Leu Arg Leu Ile Asn Thr Ser Val Gl - #u Asn His Phe Gln Val      225                 2 - #30                 2 - #35                 2 -      #40                                                                              - - Ser Leu Val Asn His Thr Met Cys Ile Ile Al - #a Ala Asp Met Val        Pro                                                                                             245  - #               250  - #               255             - - Val Asn Ala Met Thr Val Asp Ser Leu Phe Le - #u Gly Val Gly Gln Arg                  260      - #           265      - #           270                  - - Tyr Asp Val Val Ile Glu Ala Asn Arg Thr Pr - #o Gly Asn Tyr Trp Phe              275          - #       280          - #       285                      - - Asn Val Thr Phe Gly Gly Gly Leu Leu Cys Gl - #y Gly Ser Arg Asn Pro          290              - #   295              - #   300                          - - Tyr Pro Ala Ala Ile Phe His Tyr Ala Gly Al - #a Pro Gly Gly Pro Pro      305                 3 - #10                 3 - #15                 3 -      #20                                                                              - - Thr Asp Glu Gly Lys Ala Pro Val Asp His As - #n Cys Leu Asp Leu        Pro                                                                                             325  - #               330  - #               335             - - Asn Leu Lys Pro Val Val Ala Arg Asp Val Pr - #o Leu Ser Gly Phe Ala                  340      - #           345      - #           350                  - - Lys Arg Ala Asp Asn Thr Leu Asp Val Thr Le - #u Asp Thr Thr Gly Thr              355          - #       360          - #       365                      - - Pro Leu Phe Val Trp Lys Val Asn Gly Ser Al - #a Ile Asn Ile Asp Trp          370              - #   375              - #   380                          - - Gly Arg Ala Val Val Asp Tyr Val Leu Thr Gl - #n Asn Thr Ser Phe Pro      385                 3 - #90                 3 - #95                 4 -      #00                                                                              - - Pro Gly Tyr Asn Ile Val Glu Val Asn Gly Al - #a Asp Gln Trp Ser        Tyr                                                                                             405  - #               410  - #               415             - - Trp Leu Ile Glu Asn Asp Pro Gly Ala Pro Ph - #e Thr Leu Pro His Pro                  420      - #           425      - #           430                  - - Met His Leu His Gly His Asp Phe Tyr Val Le - #u Gly Arg Ser Pro Asp              435          - #       440          - #       445                      - - Glu Ser Pro Ala Ser Asn Glu Arg His Val Ph - #e Asp Pro Ala Arg Asp          450              - #   455              - #   460                          - - Ala Gly Leu Leu Ser Gly Ala Asn Pro Val Ar - #g Arg Asp Val Ser Met      465                 4 - #70                 4 - #75                 4 -      #80                                                                              - - Leu Pro Ala Phe Gly Trp Val Val Leu Ser Ph - #e Arg Ala Asp Asn        Pro                                                                                             485  - #               490  - #               495             - - Gly Ala Trp Leu Phe His Cys His Ile Ala Tr - #p His Val Ser Gly Gly                  500      - #           505      - #           510                  - - Leu Gly Val Val Tyr Leu Glu Arg Ala Asp As - #p Leu Arg Gly Ala Val              515          - #       520          - #       525                      - - Ser Asp Ala Asp Ala Asp Asp Leu Asp Arg Le - #u Cys Ala Asp Trp Arg          530              - #   535              - #   540                          - - Arg Tyr Trp Pro Thr Asn Pro Tyr Pro Lys Se - #r Asp Ser Gly Leu Lys      545                 5 - #50                 5 - #55                 5 -      #60                                                                              - - His Arg Trp Val Glu Glu Gly Glu Trp Leu Va - #l Lys Ala                                  565  - #               570                                  __________________________________________________________________________

We claim:
 1. A variant of a parent Coprinus laccase, which variant hasincreased oxidation potential and comprises a mutation in a positioncorresponding to at least one of the following positions in SEQ ID No.1:G411A,V,P,L, I,F,Y,W; G412A,V,P,L,I,F,Y,W; V409P,L,I,F,Y,W;T257A,V,P,L,I,F,Y,W; F358Y,W,I; T359A,V,P,L,I,F,Y,W; L480I,F,Y,W; L351I,F,Y,W; E473A,V,P,L,I,F,Y,W; D98A,V,P,L,I,F,Y,W; G131A,V,P,L,I,F,Y,W;D443A,V,P,L,I,F,Y,W; R260 A,V,P,L,I,F,Y,W.
 2. A variant of a parentCoprinus laccase, which variant has an altered pH optimum and comprisesa mutation in a position corresponding to at least one of the followingpositions in SEQ ID No. 1:180-181; 222-224; 257; 281-284; 352-353;357-358; 409-416; 470-490.
 3. A variant of a parent Coprinus laccase,which variant has an altered mediator efficiency and comprises amutation in a position corresponding to at least one of the followingpositions in SEQ ID No. 1:179-182; 223; 281-282; 353-358; 410-412; 472;474-475; 477-478.
 4. A detergent additive comprising a laccase variantaccording to claim 1 in the form of a non-dusting granulate, astabilized liquid or a protected enzyme.
 5. The detergent additiveaccording to claim 4, which additionally comprises one or more otherenzymes including a protease, a lipase, an amylase and/or a cellulase.6. A detergent composition comprising a laccase variant according toclaim 1 and a surfactant.
 7. The detergent composition according toclaim 6 which additionally comprises one or more other enzymes includinga protease, a lipase, an amylase and/or a cellulase.